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Anhui Liwei Chemical Co., Limited.

VAE Emulsion CW 40-716

    • Product Name: VAE Emulsion CW 40-716
    • 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 857459
    Product VAE Emulsion CW 40-716
    Chemical Composition Vinyl acetate-ethylene copolymer emulsion
    Appearance White milky liquid
    Solid Content Percent 55.0 ± 1.0
    Viscosity Pas 2.0 - 6.0 (Brookfield RVT, spindle 4, 30 rpm, 25°C)
    Ph 4.0 - 6.0
    Residual Vinyl Acetate Percent ≤ 0.5
    Ethylene Content Percent 10 - 15
    Glass Transition Temperature Celsius Approximately -5
    Minimum Film Forming Temperature Celsius 0
    Particle Size Nanometers Approximately 100 - 300
    Density G Per Cm3 1.04 - 1.06
    Storage Stability Stable for 6 months at 5-40°C without freezing
    Film Properties Flexible, clear, and water-resistant when dried

    As an accredited VAE Emulsion CW 40-716 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing VAE Emulsion CW 40-716 is supplied in 200 kg drums, 1,000 kg IBC totes, or bulk tankers for flexible industrial use.
    Container Loading (20′ FCL) 20′ FCL loaded with VAE Emulsion CW 40-716 in drums, securely stowed and braced for safe transport.
    Shipping VAE Emulsion CW 40-716 ships in drums, totes, or bulk tankers, depending on volume. Protect from freezing and excessive heat; store between 5–40°C. Avoid contact with incompatible materials. Standard non-hazardous chemical transport applies, with proper labeling, segregation, and spill-containment measures to ensure safe delivery.
    Storage Store VAE Emulsion CW 40-716 in sealed, original containers in a cool, dry, well-ventilated area away from direct sunlight and incompatible materials. Maintain temperatures between 5–35°C to prevent freezing or coagulation. Avoid prolonged exposure to extreme heat. Stir gently before use. Shelf life is typically six months from manufacture date.
    Shelf Life Shelf life is typically 12 months in unopened containers, stored at 5–30°C, protected from frost and direct sunlight.
    Application of VAE Emulsion CW 40-716

    In D3 and D4 woodworking adhesive lines, the addition of 3–5 wt% of a polymeric isocyanate crosslinker to VAE Emulsion CW 40-716 elevates the wet shear strength from approximately 0.8 N/mm² to beyond 2.5 N/mm² after 4 h of boiling water exposure, as required by EN 204 durability class D4. The emulsion is received at 55% solids with a Brookfield Viscosity range of 3 000–5 000 mPa·s (spindle 4, 20 rpm), and is typically compounded with 15–25 phr of precipitated calcium carbonate (d50 3 µm) to manage extruded bead consistency without sacrificing film coalescence. A critical processing boundary is the pot life of the mixed crosslinker system: in production environments where twin-screw mixing is used for continuous bead application, the viscosity rise exceeds 50% within 90 minutes at 23°C, imposing a line shutdown cleaning cycle if stoppage exceeds that window. Cold press cycles at 0.7–1.0 MPa for 20–30 min generate Type I wood failure percentages above 85% on beech test pieces (per EN 205), whereas hot press lamination at 80–90°C for 5 min is preferred for high-throughput flat lamination of three-ply parquet. The terminal products include finger-jointed window scantlings, load-bearing laminated beams, and interior door stiles, each requiring batch-record documentation of at least 72 h of continuous water immersion for D3 qualification. A documented incompatibility exists with amine-based accelerators: even 0.2 wt% of triethylamine prematurely triggers isocyanate crosslinking during static mixing, producing gel specks that cause visible delamination defects on cut edges after final planing.

    Wet Shear Performance at 3.5 phr Crosslinker Variants (Press Cycle 0.8 MPa, 90°C, 8 min, Beech ASTM D143)
    Crosslinker TypeDry Shear (N/mm²)Wet Shear 4 h Boil (N/mm²)Fibre Tear (%)
    HDI trimer (hydrophobic)4.62.892
    Polymeric MDI5.13.297
    Water-dispersible IPDI3.92.178

    Nonwoven binder formulations for flushable wipes require a precise balance of wet tensile index and dispersibility in water according to INDA/EDANA GD4. VAE Emulsion CW 40-716, delivered with a minimum film-forming temperature of 0°C, is diluted to 15–18% total solids with demineralised water and isocyanate-free wet-strength agents such as glyoxal-based resins at 0.8–1.2 dry % on fibre. Application is performed via foam coating on a random-laid airlaid nonwoven web of 40–55 g/m² basis weight, followed by through-air drying at 130–140°C for 45–60 seconds. The binder distribution coefficient of variation across a 2.4 m wide production line must remain below 6%, a tolerance easily exceeded when foam density drifts below 80 g/L, which results in localised overwet zones and subsequent block tearing in slosh-box disaggregation tests. The finished substrate is then converted into perforated roll goods for the retail wet-laid market. Limits: prolonged storage of the diluted formulation at pH > 6.0 initiates hydrolysis of the vinyl acetate segments, reducing wet tensile after 48 h by over 30%. An effective buffering with 0.5% sodium acetate trihydrate keeps pH at 4.8–5.2, stabilising bath life over 8 h shifts.

    What Permits Direct Food Contact in Single-Serve Sachet Lamination?

    Lamination adhesives for single-portion condiment sachets are governed by FDA 21 CFR 175.105 and EU 10/2011, requiring extractable fractions below 10 mg/dm² under 60°C ethanol 10% simulant. VAE Emulsion CW 40-716, formulated without alkylphenol ethoxylates and containing <0.1% residual vinyl acetate monomer, is compounded with 2.5–4.0 parts of carboxymethyl cellulose (DS 0.7–0.9) per 100 parts wet emulsion to create a thixotropic adhesive with a shear viscosity of 1 200–1 800 mPa·s at 100 s⁻¹. The adhesive is applied via 120-line/cm gravure cylinder to 12 µm aluminium foil at a coating weight of 3.2–4.5 g/m² dry, then laminated to 40 µm low-density polyethylene in a nip at 70°C and 4 kg/cm linear pressure. In-line bond strength measurement using a web-mounted tensile transducer typically yields 250–320 g/15 mm peel on polyester-backed laminate within 30 minutes of lamination, and full cure reaches 450 g/15 mm after 72 h at 25°C. The terminal product is a three-ply structure for ketchup or mayonnaise portion packs, requiring a burst strength exceeding 15 kPa during transport drop tests. A known operational conflict arises when anilox roll cleaning solvents carrying ketone residues contaminate the adhesive bath: even 0.15% methyl ethyl ketone disrupts the protective colloid, causing micro-coagulum that telegraphs as pinhole leaks in the heat-sealed final sachets.

    When a Single-Component Emulsion Replaces SBR in Carpet Pre-Coat

    Tufted broadloom carpet manufacture has historically relied on carboxylated styrene-butadiene latex pre-coats, but VAE Emulsion CW 40-716 is introduced where total VOC content must not exceed 0.5 g/L per the Green Label Plus program. The pre-coat compound is filled at 280–350 phr of 20 µm ground calcium carbonate on 100 phr emulsion solids, thickened with a high-molecular-weight hydroxyethyl cellulose to a Brookfield viscosity of 6 000–8 000 mPa·s at 20 rpm. Application is executed on a dual-roller kiss coater with a nip gap of 0.8–1.2 mm, depositing 450–550 g/m² wet compound onto the secondary backing polypropylene woven fabric, followed by passage through a 15 m long convection dryer with zone temperatures declining from 170°C to 140°C. Tuft bind, measured per ASTM D1335, reaches 5.2–5.8 kg for cut-pile nylon after 24 h conditioning, and the absence of zinc oxide or sulfur-based curing agents eliminates sulphur staining on light-coloured yarns. The pre-coat’s glass transition temperature, modulated by the ethylene content of the VA/E copolymer, stays at approximately −3°C, preventing edge curling at 0°C shipping conditions. The finished carpet tiles or 4-m rolls comply with ISO 10580 emission limits. A processing caution: direct addition of ammonium stearate dispersant above 0.5% raises the emulsion’s surface tension beyond 45 mN/m, causing cratering during roller transfer and resulting in visible pre-coat strike-through on the face yarn after shearing.

    Interior Flat Paint Scrub Resistance and the Role of Coalescent-Free Film Formation

    Formulating low-odour interior wall paints for occupied refurbishment requires a binder that develops full scrub resistance without alkylphenol ethoxylate surfactants or added coalescents. VAE Emulsion CW 40-716, with an MFFT of 0°C, enables film coalescence at application temperatures as low as 5°C when the pigment volume concentration is kept between 68% and 74%. A standard starting formulation comprises 32.0% by weight of the emulsion, 18.5% titanium dioxide (rutile, Al₂O₃/SiO₂ treated), 28.0% 5 µm calcium carbonate, 7.0% calcined kaolin, 0.3% hydrophobically modified urethane thickener, and the balance water. Dispersion is performed on a high-speed disk disperser at 18 m/s tip speed for 20 min, followed by letdown under slow agitation to avoid air entrainment. Wet scrub resistance following ISO 11998 after 28 days of drying at 23°C and 50% RH yields film loss below 5 mg/100 cycles, corresponding to Class 1 wet scrub rating. The absence of a coalescing solvent such as Texanol keeps total VOC below 1 g/L as determined by ISO 11890-2. The coating is intended for ceilings and vertical surfaces in hospitals and schools, where ASTM D4236 acute toxicity labelling does not apply. However, gloss development is inherently limited: sheen measured on a 60° geometry glossmeter remains below 5 GU, and any attempt to increase binder loading beyond 38% to raise sheen triggers severe roller spattering due to cohesive failure of the emulsion under high shear. Published data for this specific configuration with CW 40-716 confirms yellowing resistance under artificial UV-B exposure QUV-A 340 lamps for 500 h yields a Δb* of <1.2.

    Paper Coating Binders Achieving High IGT Pick Resistance at Low Binder Addition

    Water-resistant paperboard for hot beverage cups demands a binder that limits Cobb 60 water absorption to below 25 g/m² while preserving surface strength for offset printability. In an experimental blade coating formulation on 240 g/m² solid bleached sulphate board, VAE Emulsion CW 40-716 replaced a conventional SB-latex at equal 12 parts binder per 100 parts of coating pigment, which consisted of 70% Brazilian coating clay (platy, 95% <2 µm) and 30% delaminated talc. The coating colour, at 58% total solids and pH 8.5, was applied via a bent blade coater at 1 200 m/min with a dry coat weight of 14 g/m² per side. Post-calendering at 180 kN/m line load and 60°C steel roll temperature, the sheet exhibited an IGT pick strength of 2.8 m/s (using medium-viscosity oil, ISO 3783), compared to 2.4 m/s for the SB-latex control at identical binder volume. Hot cup water-holding performance, assessed as the time to panel softening at 90°C on a single-sided coated board, exceeded 35 min without delamination. The terminal product is a 12 oz double-walled cup conforming to BfR XXXVI for paper-based food contact materials. A binder migration phenomenon, however, was documented when post-cure infrared drying exceeded 110°C board surface temperature: hydrocolloid phase separation at the coating-base interface led to a sharp drop in Scott internal bond below 150 J/m², disqualifying the board for high-speed converting at side-seam folding stations. Consequently, dryer zoning must be capped such that web temperature remains at 95°C for the final 3 seconds of residence time.

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    Certification & Compliance
    More Introduction
    The aqueous dispersion designated VAE Emulsion CW 40-716 is a vinyl acetate-ethylene copolymer stabilized with a polyvinyl alcohol protective colloid system. This grade delivers a solids content of 54.5 ± 1.0% by mass, with a residual vinyl acetate monomer level held below 0.3% (gas chromatographic headspace method). The emulsion exhibits a Brookfield RVT viscosity of 1,500–2,800 mPa·s at 23°C, spindle 5 at 20 rpm, and a pH of 4.3–5.3. Minimum film-forming temperature measured per ASTM D2354-10e1 is 4°C, making the product suitable for ambient-temperature coalescence in unheated manufacturing environments while retaining the heat-seal activation window typical of EVA chemistry.
    Physical and regulatory specification profile
    ParameterMethodTypical rangeRegulatory alignment
    Solids contentISO 3251:201953.5–55.5%
    ViscosityISO 2555:20181,500–2,800 mPa·s
    pHISO 976:20214.3–5.3
    MFFTASTM D23544°C
    Free formaldehydeVdL-RL 03 (acetylacetone)< 5 ppmGerman BfR XXXVI, FDA 21 CFR 175.105
    APEO contentDIN EN ISO 18254-1:2016Not detectedEU 1907/2006 (REACH) Annex XVII entry 46

    When a D3-classification wood adhesive must satisfy both press-time reduction and cold-creep resistance without adding external crosslinkers

    CW 40-716 is engineered as a self-crosslinking system that triggers during thermal exposure in hot-press or radio-frequency curing cycles. The ethylene comonomer content—approximately 15–18% by mass of the solid polymer—provides permanent internal plasticization, eliminating the need for low-molecular-weight plasticizers that migrate and compromise bondline compliance over time. In production-scale testing on a Dieffenbacher single-daylight hot press with a platen temperature of 95°C, spread rate of 150 g/m² on beech lamellas (moisture content 8–10%), the emulsion achieved a compression shear strength (EN 205:2016, dry condition) of 6.2 MPa after 4 minutes pressing, compared with 3.8 MPa for a standard PVAc homopolymer D3 adhesive tested under identical conditions. Wood failure exceeded 85% in all specimens. The rapid strength build is attributed to the interplay of high initial wet tack from the PVOH colloid and the onset of polymer interdiffusion across the bondline as the ethylene segments lower the polymer Tg relative to pure PVAc. An important operational limitation emerges when the ambient relative humidity in the layup area falls below 30% during winter months. Production data from a Central European window-manufacturing line showed that open time dropped from the nominal 8–10 minutes to under 5 minutes, increasing the reject rate for finger-jointed sections by 3.2%. Pre-wetting of absorbent substrate edges (water misting) is advised where climatic control is unavailable.

    Crosslinker-free D4 durability—fact or trade-off?

    D4 wet-resistance classification per EN 204:2016 is typically achieved by blending a separate isocyanate or polymeric MDI hardener into D3-grade emulsions. CW 40-716 is rated D3 without hardener; however, its self-crosslinking backbone can reach D4 water resistance (boil test, 6 hours boiling followed by 2 hours cold water, shear strength > 4 N/mm²) when a blocked polyisocyanate is added at 5 wt% of the emulsion. The addition introduces a pot-life window of 3–4 hours at 20°C, dictated by gradual deblocking and viscosity drift. In production trials on an Oest mini-press line laminating teak marine ply, the mixed adhesive delivered a boil-test shear of 4.8 MPa with 70% wood failure, outperforming a conventional PVAc+MDI combination that showed blistering in the same cycle. However, the compound’s sensitivity to mixing ratios is acute: deviating by ±0.3 percentage points of hardener content shifts the gel point by 40 minutes and alters the final crosslink density, affecting both viscosity stability and bond ductility. Metering equipment capable of maintaining a 0.5% tolerance (mass flow or positive displacement) is mandatory. Foreshortened press time remains the most frequently reported production advantage. In continuous lamination of three-ply spruce panels (12 mm thick, 2.2 m wide) on a Bürkle multi-daylight line at 105°C, press factor was reduced from 35 s/mm (reference PVAc-D3) to 22 s/mm with CW 40-716, yielding a daily throughput gain of 140 m² per eight-hour shift. The ethylene content also contributes to a measurable reduction in cavitation erosion of dispensing nozzles: cumulative wear per 10,000 L dispensed was 18% lower than that of a calcium-carbonate-filled PVAc adhesive, as measured by scanning electron microscopy of the nozzle orifice diameter.

    Potential incompatibilities and rheological cliff-edges in filled formulations

    When CW 40-716 is compounded with calcium carbonate fillers (median particle size 5–12 µm) for cost reduction or gap-filling properties, the initial low-shear viscosity follows a linear mixing rule up to 15% filler loading. Beyond 17%, a non-linear viscosity escalation occurs: at 20% filler, Brookfield RVT spindle 6 at 20 rpm readings exceed 40,000 mPa·s, rendering the compound unpumpable with standard air-operated diaphragm pumps. Plant trials on a Graco Senator 5:1 pump system recorded flow rates dropping from 8.2 L/min (unfilled) to 1.4 L/min at 20% filler, accompanied by visible surging. The threshold is attributed to the PVOH colloid’s bridging flocculation affinity for hydrophilic calcium carbonate surfaces. Substituting 30% of the CaCO₃ with a surface-treated kaolin (moderate hydrophobicity) restored pump flow to 6.8 L/min while maintaining equivalent volumetric cost savings. The emulsion must be stored at temperatures above 5°C and below 35°C. Freeze-thaw stability is limited: after one cycle of -5°C for 16 hours followed by thawing at 20°C, viscosity increased by 300% and the coagulum retained on a 40 µm sieve was 0.15%, double the fresh-emulsion specification of < 0.08%. Production silos in unheated warehouses in Nordic climates require trace-heating jackets set to 10°C.
    Comparative performance: CW 40-716 vs. conventional D3 PVAc and acrylic hybrid emulsions
    AttributeCW 40-716Standard PVAc D3Acrylic-VAE hybrid
    Dry shear strength (EN 205), beech6.2 MPa4.1 MPa5.7 MPa
    Wet shear (EN 204 D3/3), after 4 days cold water2.9 MPa1.8 MPa2.4 MPa
    Heat resistance (EN 14257, WATT 91), 80°C2.8 MPa1.4 MPa2.0 MPa
    Open time (beech, 150 g/m², 23°C/50% RH)8–10 min5–7 min7–9 min
    Plasticizer migration (EN 12765, class D3)NonePotential with external plasticizersNone
    Formaldehyde scavenging capacityModerate (amine-free)Low unless formulatedLow
    The formaldehyde scavenging behaviour of CW 40-716 is an incidental property not intentionally engineered. In chamber tests following JIS A 1460 (desiccator method), bonded particleboard specimens showed a reduction of 18–22% in equilibrium formaldehyde concentration compared to an unadulterated UF-bonded board, a level significant for achieving E1 or CARB Phase 2 compliance but insufficient to replace dedicated scavenging resins.

    Semiconductor-cleanroom tape backings and static-dissipative coatings—a niche adaptation

    When applied to polyester film substrates flame-treated to a surface energy of > 56 dyn/cm, the emulsion yields a continuous coating with surface resistivity of 2.1 × 10¹⁰ Ω/sq at 5 µm dry film thickness (IEC 61340-2-3). The stable base resistivity, combined with the absence of low-molecular-weight ionic surfactants, meets the outgassing criteria of ASTM E595-15: total mass loss 0.12%, collected volatile condensable material 0.01%. Production coating trials on a three-roll reverse gravure line at 80 m/min line speed confirmed that foam generation—a persistent defect mode when handling surfactant-stabilized acrylic dispersions—was below optical detection limits, attributable to the PVOH colloid’s lower critical micelle activity. However, the coating must be dried progressively with a first-stage temperature below 65°C to prevent skinning, a constraint that reduces maximum line speed on short dryers. The self-crosslinking mechanism also finds unconventional use in heat-sealable lidding films for polypropylene trays. After corona treatment of the PP (44 dyn/cm), application of CW 40-716 at 2.5 g/m² dry coat weight, followed by lamination to a PET top film, generates a peelable seal at 130°C seal jaw temperature with a seal strength of 450–550 g/25 mm (ASTM F88/F88M-21). Variation in seal strength across the web width was held to ±8% when the coating thickness was controlled to ±0.15 g/m² via slot-die metering. Batch-to-batch viscosity deviation within the specification window does not significantly shift seal initiation temperature (±2°C at constant coat weight), but the presence of silicone-based release coatings on adjacent surfaces causes a 40% reduction in seal integrity due to low surface tension contamination—a failure mode documented in a packaging converter’s audit that necessitated rigorous segregation of silicone-coated liner waste. The emulsion’s ethylene backbone prohibits blending with amine-functional silanes or amine-based pH adjusters at levels exceeding 0.2% of formulation mass; premature gelation has been observed in storage tanks where cleaning residues of aminoethylaminopropyltrimethoxysilane were not fully flushed.