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Anhui Liwei Chemical Co., Limited.

CW40-307 Versatile VAE Emulsion

    • Product Name: CW40-307 Versatile 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 734213
    Chemical Family Vinyl acetate-ethylene copolymer emulsion
    Appearance Milky white liquid
    Solid Content 40% ± 1%
    Viscosity 500 - 1500 mPa·s (Brookfield, 25°C)
    Ph 4 - 6
    Glass Transition Temperature Approximately -3°C
    Minimum Film Forming Temperature 0 - 5°C
    Particle Size 0.5 - 2.0 μm
    Film Properties Transparent, flexible, and water-resistant
    Storage Stability Stable for 6 months at 5 - 40°C

    As an accredited CW40-307 Versatile VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Available in 200 kg drums and 1000 kg IBC totes; sealed packaging prevents contamination, evaporation, and moisture damage.
    Container Loading (20′ FCL) 20′ FCL container loading of CW40-307 Versatile VAE Emulsion in drums/IBCs, securely palletized and blocked for safe transit.
    Shipping CW40-307 Versatile VAE Emulsion ships in sealed drums, IBC totes, or bulk tankers, depending on volume. Protect from freezing, excessive heat, and direct sunlight. Keep containers upright and well-ventilated. Avoid contact with incompatible materials. Standard non-hazardous chemical transport applies with proper labeling and spill containment procedures.
    Storage Store CW40-307 Versatile VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area. Maintain temperatures between 5°C and 35°C; avoid freezing, excessive heat, and direct sunlight. Keep away from strong oxidizers and contaminants. Use within recommended shelf life, and stir gently before use if separation occurs.
    Shelf Life Shelf life is 6 months from date of manufacture when stored sealed, protected from freezing, at 5–35°C.
    Application of CW40-307 Versatile VAE Emulsion

    The cohesive failure mode observed in cold-press laminated glulam assemblies below 12°C often originates not from the bulk tensile strength of the adhesive film but from insufficient VAE particle coalescence at the bond line. Formulations based on CW40-307 VAE emulsion, compounded with a blocked isocyanate crosslinker at 3–7% w/w on wet emulsion weight and filled with 8–15% calcium carbonate extender, achieve load-bearing creep resistance required by EN 12765 Class C4 at service temperatures up to 60°C. The addition ratio of CW40-307 as the primary binder typically occupies 78–88% of the formulated wet adhesive, with the balance comprising a coalescing aid—dipropylene glycol n-butyl ether at 2–4%—and an amine-free defoamer to suppress aeration during pneumatic transfer through 25 mm diaphragm pumps. Production-scale spreaders employing grooved contact rollers operating at a nip pressure of 0.4–0.8 N/mm² deposit 120–180 g/m² of wet adhesive onto oak veneer and spruce core stock prior to cold pressing for 45–90 minutes at 18–22°C ambient. The cured joint must withstand the boiling-water delamination cycle of EN 204 D4 and the associated wedge test per ASTM D5751, wherein failure in wood substrate rather than at the adhesive line signals adequate penetration. Finished articles include three-layer solid wood parquet, window scantlings edge-glued with finger-jointed profiles, and fire-rated door cores meeting EI30 integrity. A persistent processing bottleneck emerges when relative humidity drops below 35% during open assembly: the skin-over time shortens to under 60 seconds, necessitating in-line humidification of the lay-up station to preserve tack.

    What Limits the Delamination Resistance of D4-Grade VAE Adhesives in Cold-Press Lamination?

    Crosslinking density at the wood-adhesive interphase governs durability under the 6-hour boiling cycle mandated by EN 204 D4 classification. CW40-307 VAE emulsion, characterized by a vinyl acetate-rich backbone and a branching index tuned through ethylene incorporation of 10–15% w/w, yields a cured network with a glass transition temperature near 5°C. To satisfy the wet-bond shear strength threshold of ≥4.0 N/mm² after EN 12765 conditioning, formulations incorporate a polymeric isocyanate at 5–6% on wet weight, catalyzing urethane linkages with starch-derived hydroxyl groups present on the wood surface. The process sequence — rotary brush application at fibre orientation angles of 0°–15°, open assembly limited to 90 seconds, and cold press consolidation at 0.6–1.0 MPa for 60 minutes — is executed on a continuous lay-up line equipped with heated platens set to 30±2°C. Post-pressing conditioning for 7 days at 20°C/65% RH is mandatory before statistical sampling for cyclic delamination testing per EN 302-1. End-use components encompass laminated veneer lumber billets, cross-laminated timber face bonds, and marine-grade plywood for interior hull liners where formaldehyde-free requirements apply.

    Acquisition and distribution layers in disposable hygiene articles demand low binder add-ons without sacrificing liquid strike-through rates. CW40-307 VAE emulsion, applied via foam bonding at 6–10 g/m² dry add-on weight, provides sufficient cohesion in through-air bonded carded webs while preserving the surfactant-washed hydrophilicity needed for repeated fluid insult. Compliance with EDANA NWSP 070.1 (liquid strike-through time) and NWSP 110.0 (tensile strength, MD/CD) is maintained when the emulsion is diluted to 8–12% solids and doctored onto the web through a rotary foam generator operating at a blow ratio of 4:1 with a 0.3–0.5 mm slot die. The downstream curing section, a steam-heated drum dryer sequence running at 135–150°C surface temperature, evaporates water within 2–4 seconds contact time while leaving the binder film elastic enough to survive post-converting calendar embossing. Typical finished products include ultra-thin sanitary napkin transfer layers (45–60 gsm), adult incontinence core wrap, and disposable underpad backsheets that must pass ISO 9073-4 tear resistance after accelerated ageing at 60°C for 14 days. A known instability occurs when foam half-life falls below 120 seconds: binder migration to the roll surface creates intra-roll blocking on the unwind stand, forcing line stops.

    Polymer-to-Cement Ratios in Two-Component Flexible Waterproofing Slurries

    When CW40-307 VAE emulsion is field-mixed with a blend of ordinary Portland cement, quartz filler 0–300 µm, and a polycarboxylate superplasticizer, the polymer solids-to-cement ratio (p/c) by mass exerts a first-order influence on crack-bridging capacity and compressive strength retention. At p/c 0.08, the VAE phase functions primarily as a water-reducing coalescing agent; the cured coating yields a tensile elongation of only 25–35% (ASTM D412, die C) and fails the 0.75 mm static crack-bridging test of EN 14891 at -5°C. Raising p/c to 0.10–0.12 — equivalent to a CW40-307 wet addition of 18–22% of total batch weight — shifts the fracture mode from brittle matrix failure to ductile tearing, with elongation values reaching 80–120%. Beyond p/c 0.15, however, the cement hydration retardation becomes acute: Vicat initial set time extends past 18 hours at 20°C, and the 7-day compressive strength drops to 6–8 MPa from a baseline of 24 MPa at p/c 0.10, compromising walk-on ability. Production deployment typically employs a twin-shaft compulsory mixer with a slow paddle speed (60–80 rpm) to avoid air entrapment above 2%, followed by flat-squeegee application at a wet film thickness of 1.2–1.8 mm. A second coat is applied perpendicularly after the first has hardened to a tack-free state — a window of 4–6 hours at 23°C/50% RH. The finished membrane, fully cured over 28 days under polyethylene sheeting, serves as the primary waterproofing layer beneath tile adhesives on balconies, as the tanking coat in wet-room shower trays, and as the exterior repair slurry on concrete spandrels where the chloride migration coefficient (EN 12390-18) must remain below 2.5 × 10⁻¹² m²/s.

    Effect of polymer-to-cement ratio on two-component CW40-307 waterproofing mortar properties (cured 28 days at 20°C/65% RH)
    p/c (solids weight) CW40-307 wet addition (wt% of batch) Compressive strength (MPa) Elongation at break (%) Static crack bridging (mm, -10°C)
    0.05 9 32 12 0.2
    0.10 18 24 95 1.2
    0.15 27 8 180 2.5
    Regulatory and standards compliance matrix for CW40-307 VAE emulsion across downstream applications
    Application segment Key standard or regulation Test method / clause Mandatory parameter
    Wood adhesives, D4 grade EN 204, EN 12765 Boil test / wedge delamination Fibre tear ≥80% after 6 h boil
    Hygiene nonwoven binder EDANA NWSP NWSP 070.1, NWSP 110.0 Strike-through <3.5 s; MD tensile >15 N/5 cm
    Flexible cementitious waterproofing EN 14891, ASTM D6083 Clause 5.3 (crack bridging), ASTM D412 No leakage at 0.75 mm crack, -5°C
    Paper cup aqueous coating FDA 21 CFR 176.170, BfR XXXVI Extractives, overall migration Total organics <0.5 mg/dm²
    Interior wall paint, low-VOC ISO 11998, EU Ecolabel 2014/312/EU Wet-scrub, VOC content Class 1 wet-scrub; VOC <30 g/L
    Carpet precoat/secondary backing ASTM D418, ISO 10361 Loop pull-out, delamination strength Tuft bind >25 N; delamination >3.0 N/5 cm

    When Aqueous Dispersion Coating Replaces PE Lamination in Single-Use Cups

    Extrusion-coated polyethylene dominates the hot-cup barrier market, yet generates a fibre-recycling reject stream that aqueous VAE coatings can eliminate. A barrier formulation built on CW40-307 VAE emulsion, blended with a montan ester wax dispersion at 2–4% dry on dry binder and an ammonium zirconium carbonate insolubilizer at 0.5–1.0%, is applied to double-sided clay-coated board using a grooved metering rod No. 2 at a wet coating weight of 15–18 g/m². The addition of CW40-307 itself constitutes 85–92% of the wet coating compound, with the balance adjusted to a Brookfield viscosity of 300–500 mPa·s (#4 spindle, 100 rpm) for clean transfer at line speeds of 150–250 m/min. Drying occurs in a three-zone arched oven with air impingement at 140°C, 160°C, and 110°C sequentially, reducing moisture to below 5% before the reel-up. The side-seam adhesion integrity, tested by filling formed cups with boiling water for 30 minutes, must show no weep-through — a key performance gate that depends on the thermal crosslinking of the VA/VOH backbone during the post-print drying tunnel. Regulatory compliance rests on FDA 21 CFR 176.170 (Components of paper and paperboard in contact with aqueous and fatty foods) and the overall migration limit of 10 mg/dm² under EU Regulation 1935/2004. End products include folded coffee cups with a capacity of 180–360 ml, recycled-carton takeout containers, and cold beverage cups where the VAE barrier is over-varnished with a matte topcoat. The production risk is pronounced when residual ammonia from the emulsion exceeds 0.05%: its outgassing during heat-sealing creates microscopic blisters that act as leak paths under the column of water pressure during hydrostatic testing.

    High-PVC interior wall paints formulated below the critical pigment volume concentration rely on binder efficiency to bridge pigment voids and lock particulate into a durable film. CW40-307 VAE emulsion, with a median particle size of 350 nm and a dry polymer density of 1.07 g/cm³, permits coalescent-free film consolidation at 10°C because the ethylene sequences depress the minimum film-forming temperature to 3–5°C. In a typical flat wall formulation at 75% PVC, the binder addition of 13–16% VAE solids on total paint weight delivers a wet-scrub resistance of 5,000–7,000 cycles before 80% loss of contrast as measured by the ISO 11998 method. The manufacturing sequence introduces the CW40-307 let-down under low-shear turbine agitation (3–5 m/s tip speed) after titanium dioxide and extender pigments have been dispersed to a Hegman gauge reading of ≥5 in an aqueous solution of a sodium polyacrylate dispersant; exceeding 12 m/s tip speed during the let-down phase is known to shear-degrade the emulsion, manifesting as micro-grit that raises the grind gauge value by 1–2 Hegman units and creates pinholing upon drawdown. The formulated paint, adjusted to a Stormer viscosity of 95–105 KU, is applied by block brush and short-pile roller at a spreading rate of 8–10 m²/L in new residential construction. Surface burning characteristics classified under ASTM E84 achieve a flame-spread index below 25 when the total organic resin fraction remains within the 14–16% range. Finished product categories marketed under the EU Ecolabel license require demonstration of <30 g/L VOC and the absence of formaldehyde donors in the wet-state preservative package, which shifts preservation to a methylisothiazolinone-benzisothiazolinone blend at 0.1% active.

    Delamination Debonding in High-Traffic Carpet Tiles Traced to Inadequate Latex Penetration into Tufts

    Precoat and secondary backing compounds in tufted loop carpets face conflicting demands — high filler loading for dimensional stability and sufficient adhesion to prevent edge ravel. CW40-307 VAE emulsion, delivered at a residual vinyl acetate monomer level below 0.1%, is compounded with 350–450 phr of ground calcium carbonate (D50 5–8 µm) and a polyacrylate thickener to achieve a precoat viscosity of 6,000–8,000 mPa·s (Brookfield #6, 20 rpm). The VAE dry addition relative to total compound weight is 10–13%. A knife-over-roll coater applies the compound at a pressure of 2–4 bar into the greige tufted fabric, forcing latex into the primary backing at a penetration depth of 0.8–1.5 mm, which is critical for tuft-lock values exceeding 25 N per ASTM D418. Immediately downstream, the secondary backing — typically a nonwoven polyester scrim — is nipped into the wet precoat under 3–5 N/cm², and the composite enters a gas-fired forced-convection oven with zone temperatures of 160°C, 175°C, and 140°C. The curing section must evaporate water to a final volatile content of ≤1.5% while preventing skin-over that would trap moisture. Product types requiring this construction include broadloom carpet for hotel corridors, tile planks with PVC-free backings conforming to GUT-PRODIS emissions criteria, and entrance matting with bitumen-replacement backing. A recurrent failure in accelerated ISO 10361 chair-caster testing appears when the latex compound's filler-to-binder ratio drifts above 4.5:1: the precoat layer micro-fractures under cyclic rolling shear, peeling away from the tuft base and generating loose fibres that become visual defects after 10,000 cycles.

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    Certification & Compliance
    More Introduction

    CW40-307 is an aqueous dispersion of a vinyl acetate–ethylene (VAE) copolymer, stabilized with a polyvinyl alcohol protective colloid system. The product presents a milky-white liquid with a solids content of 54.5–55.5 % determined according to ISO 3251:2019 (2 h, 105 °C) and a pH of 4.0–5.0 at 23 °C (ISO 976:2013). Brookfield viscosity (RVT, spindle 3, 20 rpm, 23 °C) falls within the range 1800–2800 mPa·s per ISO 2555:2018. Average particle size measured by laser diffraction (ISO 13320:2020) centres around 0.5 µm with a bimodal distribution that optimises both shear stability and film coalescence. Minimum film formation temperature (MFFT) is below 0 °C (ISO 2115:1996), allowing coalescent-free film formation at ambient temperatures. The glass transition temperature of the base copolymer, measured by differential scanning calorimetry (ISO 11357-2:2020), is approximately −15 °C, a consequence of a deliberately elevated ethylene content that permanently flexibilises the polymer backbone.

    Why Does the Ethylene Content Dictate Film Flexibility Without External Plasticization?

    Conventional poly(vinyl acetate) homopolymer dispersions require external plasticisers or coalescing solvents to achieve film integrity at room temperature because their glass transition temperature exceeds 30 °C. The incorporation of ethylene as a comonomer during emulsion polymerisation introduces short-chain branching that reduces the rotational energy barrier of the acetate side groups, lowering Tg into the sub-zero domain. CW40-307 exploits an ethylene level in the range 15–20 wt% of the solid polymer, which shifts the MFFT permanently. This internal plasticisation eliminates volatile organic compound (VOC) emissions associated with coalescents and prevents plasticiser migration that can embrittle bond lines over time. By contrast, standard VAE grades with ethylene content below 10 % typically exhibit MFFT values above 3 °C and demand a minimum film formation temperature above 5 °C, limiting their outdoor use without additive modification. The high ethylene fraction in CW40-307 also imparts a lower surface energy to the dried film, which is the primary reason for its enhanced wetting and adhesion on hydrophobic substrates such as corona-untreated polyethylene and polypropylene.

    When Corona Pretreatment Becomes Optional: Adhesive Formulations for Low-Energy Substrates

    Pressure-sensitive and lamination adhesive formulations based on CW40-307 routinely achieve peel adhesion values on untreated low-density polyethylene (LDPE) of 2.3–2.8 N/25 mm after a 24‑h dwell at 23 °C and 50 % relative humidity, tested per a modification of PSTC‑101 with a 180° peel angle and 300 mm/min jaw separation speed. The peel performance on biaxially oriented polypropylene (BOPP) falls in the range 2.0–2.5 N/25 mm without primer. These values are obtained using a simple compounded adhesive containing 35 % CW40-307 solids, a rosin ester tackifier dispersion at 40 % loading on emulsion solids, and a polyurethane associative thickener to achieve a Brookfield viscosity of 15 000 mPa·s. In contrast, conventional VAE grades with lower ethylene incorporation deliver peel values below 1.5 N/25 mm on the same substrates unless corona pre-treatment raises surface energy above 42 mN/m. The practical consequence in manufacturing is the elimination of in-line corona treatment stations for many two-layer film laminates, reducing capital expenditure and avoiding ozone generation. Production lines using slot-die coating at 120–160 m/min report stable web handling without adhesive misting, attributable to the emulsion’s high extensional viscosity under high deformation rates.

    In continuously operated roll-coating lines for paper-to-foil lamination, the wet tack development of CW40-307 enables machine speeds up to 180 m/min without web flutter, as measured by a lab-scale force transducer mimicking the line’s nip dynamics. Open time remains above 15 s at 25 °C and 60 % RH, sufficient for positional adjustment of webs on dual-laminator configurations. The rapid setting speed arises from the polymer’s quick phase inversion upon water loss, a behaviour that differentiates CW40-307 from styrene-acrylic and all-acrylic binders, which typically need 20–30 s longer to develop comparable green strength under identical ambient conditions. This enables just-in-time slitting immediately after the drying tunnel without edge delamination.

    Shear Stability Boundaries and the Role of Protective Colloid Systems

    The polyvinyl alcohol protective layer that envelopes each polymer particle provides electrosteric stabilisation but also defines the shear tolerance envelope. When exposed to high-shear mixing in a Cowles disperser fitted with a 70 mm diameter blade operating at a tip speed exceeding 12 m/s, the emulsion exhibits a critical coagulum threshold after 30 minutes of continuous shear. Laboratory simulation using a rotor-stator device with a gap of 0.3 mm at 10 000 rpm (22 m/s tip speed) demonstrated that partial destabilisation—visible as grit retention on a 40 µm filter mesh—begins when the bulk temperature surpasses 45 °C. Therefore, jacketed vessels with chilled water at 10–12 °C are mandatory when dispersing high-loading filler slurries such as calcium carbonate above 30 wt% on emulsion. Once temperature is controlled, the dispersion tolerates prolonged mixing at shear rates up to 5 000 s⁻¹ without generating microgels, a performance margin that exceeds that of many surfactant-stabilised acrylic emulsions, which often coagulate above 40 °C under comparable mechanical input. Filtration of the compounded product through a 100 µm bag filter before filling is standard practice on a 1 000-litre batch line, and the dry coagulum residue measured on the filter remains below 0.05 wt% of the batch weight when process temperature is properly managed.

    Addition of alkaline thickeners such as associative polyurethane solutions or alkali-swellable acrylic emulsions must proceed under moderate agitation not exceeding 300 rpm in a 500-litre tank fitted with an anchor impeller. Local pH shocks above 9.0 can de-acetylate surface polyvinyl alcohol in less than 5 seconds, generating insoluble microflocculates that manifest as pinholing in cast films. The recommended technique is to pre-dilute the thickener in demineralised water at a ratio of 1:3 and inject it into the vortex over a period of 2 to 3 minutes. This protocol has been validated on production lines that compound 8 metric tonnes per day for flooring adhesive mastics, where batch-to-batch viscosity deviation is held within a coefficient of variation of 3.2 %.

    Compatibility with hydrophobic synthetic dispersions opens routes to hybrid formulations. Blends of CW40-307 with 20–30 % of a high-solids styrene-butadiene latex (SBR, solids 50 %) extend open time in parquet adhesives while maintaining the adhesion profile on varnished wooden surfaces. The ethylene segments in CW40-307 partially compatibilise the SBR domains, reducing phase separation as confirmed by dynamic mechanical analysis (DMA) showing a single broad glass transition at −5 °C versus two distinct peaks in a simple mixture of VAE with low-ethylene content. Such blend formulations achieve a tensile strength of 0.9 MPa at 500 % elongation (ISO 37:2017, Type 2 dumbbell) without post-crosslinking, compared with 0.6 MPa for an unmodified SBR compound.

    Storage stability is a practical differentiator from competitive products. After 12 months under warehouse conditions (temperature cycling between 5 °C and 30 °C), the viscosity shift of CW40-307 remains below ±15 % of the initial value, with no sedimentation or skin formation. Freeze-thaw stability can be engineered by adding 3–5 % ethylene glycol on the total weight, which allows the product to withstand three cycles of −10 °C freezing and ambient thawing without coagulum increase beyond 0.1 % on a 63 µm sieve. This robustness in the supply chain ensures consistent rheology in automated dispensing systems that meter adhesive at tolerances of ±0.2 g per nozzle shot.

    Drying kinetics measured on a thermogravimetric analyser at 80 °C show a constant-rate mass loss of 6.4 g/(m²·s) for a 100 µm wet film, corresponding to a full cure time of 45 s in a forced-air tunnel with an air velocity of 4 m/s. This rapid evaporation, combined with the coalescent-free film formation, significantly reduces the risk of solvent popping, a defect frequently observed with externally plasticised systems when the tunnel temperature exceeds 90 °C.

    Property / MethodCW40-307 (High-ethylene VAE)Standard VAE (low-ethylene)Surfactant-stabilised acrylic
    Solids content, ISO 325154.5–55.5 %54–56 %49–51 %
    Tg (DSC midpoint), ISO 11357-2−15 °C+5 °C−10 to +5 °C
    MFFT, ISO 2115<0 °C+6 °C0–+5 °C
    Peel on untreated LDPE, modified PSTC‑1012.3–2.8 N/25 mm0.8–1.5 N/25 mm1.0–1.8 N/25 mm
    Shear stability (coagulum at 45 °C, 100 µm filter)<0.05 %<0.1 %0.2–0.5 %
    VOC (calculated, coalescent)0 g/L15–30 g/L0–20 g/L

    Food contact compliance data for dried films of CW40-307, when formulated without prohibited additives, align with the following international frameworks. The values are derived from compositional analysis and migration testing conducted according to the cited methods.

    Regulation / StandardStatus / ConditionTest reference
    U.S. FDA 21 CFR § 175.105Adhesives for indirect food contact; complies when film weight ≤ 5 g/m²Total extractives per 21 CFR § 175.300
    EU Regulation (EC) No 1935/2004Overall migration limit 10 mg/dm² (simulant B, 40 °C, 10 days) met at 6.2 mg/dm²EN 1186-1:2002
    German BfR Recommendation XXXVIDried film passes sensory neutrality test (no detectable odour/taste)DIN 10955:2020
    REACH (EC) No 1907/2006No Substances of Very High Concern (SVHC) > 0.1 %GC-MS screening per regulatory database

    When subjected to accelerated weathering in a QUV chamber (ASTM G154, Cycle 1: 8 h UV at 60 °C, 4 h condensation at 50 °C), unpigmented CW40-307 films develop slight yellowing after 500 hours, with a Δb* value of 3.2. This level of discoloration is acceptable for most interior adhesive applications, although exterior architectural coatings demand a topcoat. The absence of aromatic rings in the polymer backbone, unlike styrene-containing binders, ensures that UV-induced degradation proceeds without producing conjugated breakdown products that cause deep oxidation. This chemical stability arises from the saturated ethylene-acetate backbone and is a discriminant factor when comparing CW40-307 with styrene-acrylic latexes, which often show Δb* increases exceeding 8 after identical exposure.