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Anhui Liwei Chemical Co., Limited.

Low Ethylene VAE Emulsion

    • Product Name: Low Ethylene 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 706386
    Appearance Milky white liquid
    Solid Content 55 ± 1 %
    Viscosity Brookfield 25 C 20 Rpm 800 - 1500 mPa·s
    Ph 5.0 - 7.0
    Density 25 C 1.05 g/cm³
    Average Particle Size 0.5 - 1.5 μm
    Glass Transition Temperature Tg -5 °C
    Minimum Film Forming Temperature Mfft 0 °C
    Ethylene Content Low (5 - 15 %)
    Residual Vinyl Acetate Monomer < 0.1 %
    Mechanical Stability Good
    Storage Stability 6 months at 5 - 35 °C

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

    Packing & Storage
    Packing Low Ethylene VAE Emulsion is supplied in 200 kg polyethylene-lined steel drums or 1000 kg IBC totes.
    Container Loading (20′ FCL) Load 20′ FCL with Low Ethylene VAE Emulsion in IBCs/drums, securely braced, protected from heat/moisture, with adequate ventilation.
    Shipping Low Ethylene VAE Emulsion is shipped in sealed drums, totes, or tankers to prevent contamination and moisture loss. Protect from freezing and extreme heat; store upright in a cool, dry area. No special hazard classification applies, but proper labeling and secure handling ensure safe, stable transit.
    Storage Store Low Ethylene VAE Emulsion in sealed, corrosion-resistant containers under cool, dry conditions (5–35°C). Protect from freezing, direct sunlight, and extreme heat. Maintain good ventilation and keep away from ignition sources. Stir before use if separation occurs. Under proper storage, shelf life is typically 6–12 months.
    Shelf Life Shelf life is typically 6 months from manufacture when stored sealed, protected from freezing, and kept below 35°C.
    Application of Low Ethylene VAE Emulsion

    In millwork lamination operations where the finished joint must satisfy the D3 durability class of EN 204 and the associated shear-strength protocol of EN 205, a low-ethylene VAE emulsion with 50–55% solids and a pH of 4.0–5.5 measured by ISO 976 is metered into a jacketed mixing vessel equipped with a high-shear disperser. The wet adhesive compound is formulated at 76–84 wt% emulsion solids content, with 0.5–1.5 wt% polyvinyl alcohol protective colloid stabilizer, 1.0–2.0 wt% of a phthalate-free ester plasticizer, and 1.0–2.5 wt% fumed silica rheology modifier; final Brookfield viscosity is adjusted to 12,000–18,000 mPa·s per ISO 2555:2018, spindle 4 at 20 rpm. On production lines, adhesive transfer is performed through slotted nozzle applicators at 0.6–1.2 MPa air pressure, followed by cold pressing at 0.7–1.5 MPa for 20–45 min; for high-frequency curing, a 27.12 MHz RF press with plate temperature ramping to 60–80 °C reduces press time to 4–10 min. The operational boundary is the D4 exterior class: low-ethylene VAE compounds without a blocked isocyanate or aluminum chloride crosslinker do not sustain boiling-water immersion or cyclic water exposure, and a formulated D3 product should not be downgraded to D2 or D1 without adjusting filler loadings. Terminal product types include edge-glued solid wood panels, laminated door stiles, window scantlings, and veneer-laminated curved furniture components.

    What Constrains Scrub Resistance and Blocking in Low-Emission Interior Wall Paints?

    In interior architectural coatings, the use of a low-ethylene VAE dispersion as the main binder places simultaneous constraints on minimum film-forming temperature and block resistance; the dispersion typically exhibits a glass transition temperature of 10–20 °C and an MFFT of 5–12 °C when tested by ISO 2115. In a semi-gloss or eggshell formulation at 20–30% pigment volume concentration, the binder addition is typically 13–22 dry wt% on total paint weight, while matte wall paints may run at 10–16 dry wt%; coalescent demand is held at 0.5–2.0 wt% on total paint to maintain low-VOC classification under EU Directive 2004/42/EC and CDPH Standard Method v1.2. Manufacturing is completed on a high-speed disperser with a tip speed of 12–20 m/s for pigment dispersion, followed by a reduced-speed letdown phase at 6–9 m/s; the low-ethylene VAE is post-added because shear above 2,500 rpm can destabilize the dispersion in the presence of amine-based wetting agents. Wet scrub resistance is assessed under ISO 11998, and paints are formulated to maintain a thickness loss below 5 µm after 200 cycles when referenced to EN 13300; addition of nitrile rubber or acrylic soft-phase modifiers above 3 wt% improves low-temperature film integrity but reduces block resistance. Terminal product types include interior wall and ceiling paints, low-odour renovation paints, and alkali-resistant primers for gypsum and previously painted substrates.

    Two-component polymer-modified cementitious slurries used for balcony and wet-room waterproofing are typically produced by combining a liquid low-ethylene VAE dispersion with a dry blend of CEM I 42.5 R or CEM II/A-L 42.5 N cement, graded quartz sand, and cellulose ether. In tile adhesive dry mixes, the polymer solids addition is between 3.0% and 6.0% by dry cement mass, whereas in flexible slurry-applied waterproofing membranes the liquid polymer-to-cement ratio by weight is 0.25–0.40, producing a fresh mortar viscosity of 80,000–120,000 mPa·s at 20 rpm by ISO 2555. Compliance for thin-bed mortars is anchored to EN 12004 classifications C1T or C2E, with hydration under 23 °C/−50% RH for 28 days before tensile adhesion testing; waterproofing slurries are evaluated under EN 14891 for water impermeability and crack bridging, with a typical crack-bridging requirement of 0.75 mm at −10 °C. Production lines use forced-action pan mixers or twin-shaft paddle mixers at 180–300 rpm, and batch-to-batch variation in air entrainment is controlled by adding 0.05–0.20 wt% of a mineral oil defoamer. The main process conflict is polymer-cement ratio: raising the liquid modifier above 0.45 to improve adhesion can prolong setting time and increase air content beyond 8%, while reducing it below 0.20 impairs flexibility and crack-bridging capacity. Terminal finished goods include large-format porcelain tile adhesives, self-smoothing underlayments, and flexible cementitious waterproofing membranes for wet rooms and balconies.

    Paperboard Lamination and Direct Food-Contact Adhesion under 21 CFR 175.105

    Paper and board converting operations utilize low-ethylene VAE emulsions as high-speed side-seam and lamination adhesives because the low ethylene content yields a harder adhesive film with reduced cold flow and clean machining on rotary equipment. The emulsion is formulated at 85–92 parts per 100 wet adhesive, diluted with water to a running viscosity of 400–900 mPa·s per ISO 2555, and stabilized with 0.2–0.6 wt% of a nonionic surfactant; direct food-contact compliance is assessed under FDA 21 CFR 175.105 for adhesives, 21 CFR 176.170 for paper and paperboard components in contact with aqueous and fatty foods, and the migration limits of EU 10/2011 for plastics and articles intended for food contact. On production lines, application is performed by wheel or roller coaters running at 150–350 m/min, with nip pressures between 0.2 and 0.5 MPa; side-seam stations on carton forming machines use 0.3–0.8 mm nozzle orifices and 0.4–0.8 MPa adhesive pressure, with open time controlled between 8 and 30 s. The key operational limitation is water resistance: unmodified low-ethylene VAE seams soften under prolonged wet contact above 40 °C, and for ice-water immersion or oily food packaging the converter must add 0.5–1.5 wt% glyoxal-based crosslinker or move to a higher-ethylene VAE. Terminal product types include spiral-wound paper tubes, paper bag bottom seams, folding carton side seams, and paper cup overwrap lamination where the adhesive layer is not the primary direct food-contact barrier.

    When Nonwoven Tensile Retention Outweighs Drape and Softness

    Airlaid and carded nonwoven producers select low-ethylene VAE dispersions when the finished web must retain tensile strength after humid ageing and when stiffness is an acceptable trade-off for lower creep. The binder is applied at 12–25 g/m² dry add-on to fiber mass, corresponding to 14–28% binder solids by finished web weight, depending on fiber denier and web density; the dispersion is adjusted to 150–400 mPa·s and applied by foam impregnation or spray bar, followed by through-air drum drying at 130–150 °C for 45–120 s. Compliance is tested under ISO 9073-3 for tensile strength and elongation, ISO 9073-4 for tear resistance, and OEKO-TEX Standard 100 for skin-contact chemical limits; humid ageing is evaluated by conditioning specimens at 90% RH and 35 °C for 24 h before tensile testing. The production bottleneck occurs in foam application: a low-ethylene VAE with a surface tension below 38 mN/m may generate macro-foam that destabilizes the web, and foam density is maintained at 150–250 g/L through rotor-stator foam generators equipped with 0.3–0.5 mm perforated screens. Unlike high-ethylene VAE grades, elongation at break in the bonded nonwoven is typically below 20%, making the binder unsuitable for soft hygiene top sheets or high-drape medical fabrics. Terminal product types include automotive hoodliner and interior acoustic mats, vacuum cleaner bag support layers, filtration media edge seals, and furniture dust-cover substrates where dimensional stability is prioritized over softness.

    Carpet Tile Precoat Rheology after 400 phr Calcium Carbonate Addition

    In carpet tile and broadloom secondary-backing operations, low-ethylene VAE emulsions function as filler-bonding precoat bases because they tolerate high loadings of calcium carbonate without severe viscosity collapse. A production-grade precoat compound is built at 250–450 phr calcium carbonate per 100 phr dry emulsion solids, with 0.3–0.8 wt% polyacrylate dispersant, 0.05–0.15 wt% ammonia for pH adjustment to 8.5–9.5, and 2.0–5.0 wt% styrene-butadiene latex to recover tuft bind. Viscosity is brought to 5,000–9,000 mPa·s per ISO 2555, spindle 4 at 20 rpm, and the compound is applied by knife-over-roll or slot-die coating at 300–800 g/m² wet add-on, then dried in a stenter at 140–170 °C for 5–10 min. Compliance requirements for finished carpet include CDPH Standard Method v1.2 for VOC emissions and CRI Green Label Plus limits; halogenated flame retardants are excluded in formulations intended for EU REACH and EN 1307 performance classification. On production lines, the main failure mode is precoat strike-through: when calcium carbonate loading exceeds 450 phr, the high-shear viscosity under a 3,000 s⁻¹ shear rate drops below 1,200 mPa·s, causing penetration into the carpet pile and hardening of the finished tile. The dispersion therefore retains use only where filler levels are controlled by continuous gravimetric dosing and where the carpet backing is closed enough to accept 300–500 g/m² wet films. Terminal product types include carpet tile secondary backings, entrance mat backings, and automotive carpet precoats that must resist edge raveling during die cutting.

    Gravure and rod coating stations in flexible packaging plants employ low-ethylene VAE emulsions as peeling adhesives for wet lamination and cold-seal release substrates, where the applied film must be tack-free after drying and must not activate below 60 °C. The dispersion is diluted to 30–45% solids with deionized water, blended with 1.0–2.5 wt% propylene glycol to control open time, and coated at 2.0–5.0 g/m² dry coat weight using 180–250 lpi gravure cylinders or 3–8 µm wire-wound rods; line speeds are typically 80–200 m/min, with dryer tunnel temperatures staged from 60 °C to 95 °C. Regulatory compliance for the coated film is assessed under EU No 1935/2004 for food contact materials when the structure is used in food packaging, with specific migration testing performed according to EU 10/2011; in non-food industrial packaging, the main requirement is the German BfR XXXVI recommendation when the adhesive is not separated from food by a functional barrier. The production bottleneck is foam generation in the coating pan: line operators must hold wet surface tension above 35 mN/m and use enclosed doctor chambers to prevent viscosity increase beyond 200 mPa·s during long runs. Because low-ethylene VAE has a higher storage modulus above 60 °C, the resulting bond resists blocking in roll storage but exhibits reduced heat-seal compatibility; it is therefore specified for pressure-sensitive release coatings and lamination tie layers rather than peelable heat-seal lids. Terminal product types include cold-seal packaging bases, printed film lamination adhesives, label overwrap tie layers, and heat-sealable blister card coatings where the sealing temperature is provided by a separate lacquer.

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    Certification & Compliance
    More Introduction

    The product line designated LE-VAE 1490 comprises carboxylated low-ethylene vinyl acetate-ethylene copolymer emulsions stabilized with a poly(vinyl alcohol) protective colloid and an anionic surfactant package. Ethylene incorporation is controlled within 4–8 wt% on dry polymer, as determined by internal FTIR calibrated against reference copolymers. Representative physical properties for model LE-VAE 1490 include solids content of 54–56% per ISO 3251:2008, Brookfield viscosity of 2,000–4,000 mPa·s at 25°C using spindle 3 at 20 min⁻¹ per ISO 2555:2018, pH 4.5–5.5 per ISO 976:2013, minimum film formation temperature of 0–5°C per ISO 2115:1996, and density of 1.07–1.09 g/cm³ per ISO 2811-1:2016. The glass transition temperature measured by differential scanning calorimetry according to ISO 11357-2:2020 falls between 2°C and 8°C. Volatile organic compound content is typically below 1.0 g/L when measured by EPA Method 24, which supports formulation of indoor adhesives and architectural coatings subject to low-emission requirements.

    PropertySpecificationTest Method
    Appearancewhite to off-white liquidvisual inspection
    Solids content54–56%ISO 3251:2008
    Brookfield viscosity2,000–4,000 mPa·sISO 2555:2018, RVT spindle 3, 20 min⁻¹, 25°C
    pH4.5–5.5ISO 976:2013
    MFFT0–5°CISO 2115:1996
    Density1.07–1.09 g/cm³ISO 2811-1:2016
    Glass transition temperature2–8°CISO 11357-2:2020
    VOC content< 1.0 g/LEPA Method 24

    The product is supplied as an anionic dispersion with a narrow particle size distribution, typically 0.2–0.6 µm mean volume diameter by laser diffraction. Because the emulsion is carboxylated, neutralization with weak alkali to pH 6.5–7.5 increases mechanical stability during pigment grinding and produces pseudoplastic flow. Formulation pH should remain below 8.0 to limit saponification of vinyl acetate units and below 4.0 to prevent hydrolysis-induced viscosity drift.

    Why Does Ethylene Content in the 4–8 wt% Range Shift Film Formation and Adhesive Set Speed?

    Low ethylene incorporation disrupts chain packing of the vinyl acetate backbone without fully suppressing the polar character of the continuous film. The resulting glass transition range of 2–8°C permits ambient film formation with coalescent demand limited to 0–2 wt% on binder solids, whereas poly(vinyl acetate) homopolymer with a glass transition range of 28–40°C typically requires external plasticizer or coalescent addition above 5 wt%. The minimum film formation temperature of 0–5°C measured by ISO 2115:1996 means that model LE-VAE 1490 produces continuous films at standard plant conditions without forced-air heating, provided substrate temperature remains above 5°C. In adhesive applications, the low ethylene content limits internal plasticization relative to high-ethylene grades, resulting in higher cohesive strength and faster set speed on porous paper and board. The vinyl acetate-rich segments retain hydrogen-bonding capacity with cellulosic substrates, which contributes to peel and shear development under light compression. Published technical data for low-ethylene VAE dispersions in pressure-sensitive applications indicate that loop tack and peel are lower than high-ethylene VAE tackifier-modified systems, but static shear resistance at 60°C is higher. Specifically, a 25 mm × 25 mm overlap on stainless steel can withstand a 500 g static load for more than 24 h when the dried film thickness is controlled between 30–50 µm. The formulation should not be plasticized with phthalate esters above 5 wt% on dry polymer because excessive plasticizer migration causes loss of heat resistance and soft creep under load.

    For laminating adhesives bonding cellulose acetate or primed PET to paperboard, low ethylene VAE emulsions are applied at dry coat weights between 3–6 g/m². Wet tack develops after initial water removal and is sufficient to hold web tension on a laminating line running at 60–120 m/min. Publication of production-scale data for this specific configuration is limited, but converter line trials show that green bond strength at 2 minutes after nipping is typically adequate to prevent tunnel delamination at slitting. The operational boundary is the drying capacity of the tunnel; residual moisture above 2–3% in the adhesive layer before rewinding reduces immediate shear and permits blocking under wound tension.

    High-Shear Dispersion Response and pH Buffer Requirements for Filled Systems

    Carboxylated low-ethylene VAE emulsions tolerate high-shear mixing under controlled pH and temperature. In filled architectural coatings, the emulsion is typically let down after a pigment paste containing calcium carbonate, kaolin, or titanium dioxide has been dispersed under a 450 mm Cowles blade at tip speeds of 18–25 m/s. Direct addition of the emulsion to high-pH millbases above 9.0 can produce irreversible grit and viscosity loss due to neutralization of the carboxylated stabilizer. For production-scale dispersion, the millbase should be cooled to below 40°C before binder addition. Batch-to-batch viscosity variation on a 2,000 L high-speed disperser is reported as approximately ±500 mPa·s when the same pigment volume concentration and dispersant dosage are maintained. The recommended dispersant is an ammonium or sodium polyacrylate at 0.3–0.8 wt% on total pigment. Excessive dispersant above 1.2% reduces scrub resistance and increases water sensitivity of the dried film.

    Hard water containing more than 300 ppm calcium carbonate equivalents can destabilize the anionic system during dilution. If plant water hardness exceeds this value, chelating agents such as tetrasodium EDTA at 0.1–0.2 wt% on total formulation should be added before the emulsion. Viscosity response to pH adjustment is most linear between pH 6.8 and 7.8; beyond pH 8.0, the dispersion undergoes progressive saponification, generating free acetate ion and increasing the risk of amine odor development in stored paint. Low-shear Brookfield viscosity at 25°C after neutralization of a 35 wt% calcium carbonate-filled system is commonly 8,000–15,000 mPa·s, while high-shear viscosity measured with a cone-and-plate viscometer at 10,000 s⁻¹ remains below 300 mPa·s. The resulting shear-thinning profile permits roller application without excessive spatter.

    Differences From High-Ethylene VAE and Acrylic Emulsions Are Quantified Through Thermal and Adhesive Testing

    Low-ethylene VAE emulsions occupy a performance window between vinyl acetate homopolymers and high-ethylene VAE grades. The ethylene comonomer content of 4–8 wt% gives internal plasticization and eliminates the need for fugitive coalescents, while retaining the polar adhesion characteristics absent in more ethylene-rich copolymers. High-ethylene VAE grades with 10–20 wt% ethylene exhibit lower glass transition temperatures, typically below 0°C, and greater elongation but lower tensile strength and heat resistance. In direct comparison, model LE-VAE 1490 produces higher shear adhesion failure temperature and faster development of paper tear under ambient conditions. The trade-off is reduced low-temperature flexibility and lower peel on nonpolar surfaces without tackifier modification.

    ParameterLow-ethylene VAEHigh-ethylene VAEPVAc homopolymerAcrylic emulsion
    Ethylene content4–8 wt%10–20 wt%0 wt%not applicable
    Glass transition range2–8°C-15–0°C28–40°C-10–30°C
    MFFT by ISO 21150–5°C< 0°C12–18°C0–10°C
    Elongation at break by ISO 527-2300–600%600–1000%10–50%200–500%
    Tensile strength by ISO 527-26–12 MPa2–5 MPa15–25 MPa8–15 MPa
    Water whitening resistancemoderatelow to moderatemoderatehigh
    UV and alkali resistancelow to moderatelowlowhigh

    The comparative ranges above are representative published values for anionic-stabilized dispersion films tested under ambient conditioning. Low-ethylene VAE is therefore selected when adhesion to cellulosic surfaces, set speed, and heat resistance outweigh exterior durability and low-temperature flexibility. Acrylic emulsions remain preferable for exterior topcoats where UV exposure and wet adhesion on chalky substrates are critical, but acrylic binders generally require higher coalescent loadings to achieve low-temperature film formation and can exhibit lower wet tack on paper and board laminating lines.

    When Low Ethylene VAE Emulsion Replaces Styrene-Acrylic in Construction Admixtures

    In cementitious patching compounds and polymer-modified tile adhesives, low-ethylene VAE emulsions are introduced as the liquid polymer fraction at polymer-cement ratios of 5–15% by mass. Compared with styrene-acrylic dispersions commonly used in mortar modification, low-ethylene VAE provides higher early wet tack and better compatibility with cellulose ethers. However, the vinyl acetate backbone is more prone to alkaline hydrolysis at cement pH above 12, so open time extension requires controlled admixing and preferably the addition of the emulsion after initial cement hydration. The emulsion should be combined with potable water at 15–25°C; immediate gelling can occur if the dispersion is added to high-alkali cement slurry faster than 5 L/min in a continuous mortar mixer. Field data from twin-shaft continuous mixers indicate that delayed polymer addition produces homogeneous paste with limited latex flocculation. After 28 days, tensile adhesion of a modified patching compound to concrete by ASTM C1583/C1583M-13 typically exceeds 0.5 MPa, but published comparative data for low-ethylene VAE versus styrene-acrylic in self-leveling underlayments remain limited.

    For interior skim coats and wall compounds, low-ethylene VAE imparts moderate flexibility and blocks less than PVAc homopolymer while maintaining sanding behavior similar to harder styrene-acrylic compounds. The formulation must be protected against microbial contamination during storage because the anionic emulsion contains no built-in biocide above industrial preservation thresholds. If the compounded product is stored above 35°C for more than 30 days, viscosity drift and free acetic acid generation can increase, requiring buffering with sodium bicarbonate at 0.05–0.1 wt%. Avoid combining the emulsion with amine-functional silanes or ammonia before pH stabilization; premature neutralization above pH 8.5 accelerates acetate hydrolysis and can produce surface tack after film drying. Store in closed vessels at 5–35°C; freezing at or below 0°C causes irreversible destabilization and grit formation upon thawing.