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Anhui Liwei Chemical Co., Limited.

Dairen DA-142 VAE Emulsion

    • Product Name: Dairen DA-142 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 354709
    Product Name Dairen DA-142 VAE Emulsion
    Appearance White milky liquid
    Solid Content 54.5 ± 1.0%
    Viscosity 4000 - 6000 cps (at 25°C)
    Ph 4.5 - 6.0
    Glass Transition Temperature -5 °C
    Minimum Film Forming Temperature 0 °C
    Particle Size 0.4 μm
    Specific Gravity 1.07 (at 25°C)
    Surface Tension 35 dynes/cm
    Residual Vinyl Acetate Monomer < 0.5%
    Film Character Clear and flexible
    Mechanical Stability Excellent
    Storage Stability Good (6 months at 20-30°C)

    As an accredited Dairen DA-142 VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Dairen DA-142 VAE Emulsion is supplied in sealed plastic-lined drums, typically 200 kg net weight per drum, with custom packaging options available.
    Container Loading (20′ FCL) 20′ FCL container loading of Dairen DA-142 VAE Emulsion: palletized drums/IBCs, secured, no mixing, proper ventilation, intact seals, safe transport.
    Shipping Dairen DA-142 VAE Emulsion ships in sealed drums or bulk containers, protected from freezing and direct sunlight. Maintain temperatures above 5°C to prevent coagulation. Ensure proper labeling, ventilation, and spill containment. Avoid contact with skin and eyes; use PPE during handling. Transport as non-hazardous aqueous emulsion with standard industrial safeguards.
    Storage Store Dairen DA-142 VAE Emulsion in sealed original containers in a cool, dry, well-ventilated area between 5–35°C. Protect from direct sunlight, frost, and extreme heat. Avoid contamination by keeping containers closed when not in use. Stir gently before use and follow the manufacturer’s shelf-life guidelines.
    Shelf Life Shelf life is 12 months from manufacture when stored in original sealed containers at 5–35°C, protected from freezing.
    Application of Dairen DA-142 VAE Emulsion

    Production-scale roll-to-roll laminators processing 80–120 g/m² kraft liner to water-wettable substrates demand adhesive wet tack thresholds that prevent ply delamination within 0.2–0.8 seconds after nip contact. DA-142, a carboxylated vinyl acetate-ethylene copolymer dispersion with a sub-zero minimum film formation temperature, enables a dry bond formulation that can be diluted to 40–48% solids without coagulation during continuous recirculation through a Nordson slot-die coater. Pretreatment of the paper surface is rarely required when surface energy exceeds 38 dynes/cm; nevertheless, an inline corona discharge at 2–4 kW reduces pinholing on high-density clay-coated boards. The compounded adhesive, typically containing 0.8–1.5 wt% ammonium zirconium carbonate crosslinker on emulsion solids and 0.05 wt% ethoxylated acetylenic diol defoamer, is applied at a coat weight of 3–5 g/m² dry. A three-zone drying tunnel set to 105°C inlet, 85°C midpoint, and 60°C final stage drives off water before the webs meet at a heated steel-rubber nip maintained at 1.8–2.2 N/mm linear pressure. Post-cure proceeds on the roll over 24–48 h at ambient humidity, developing final T-peel adhesion exceeding 2.5 N/15 mm when tested according to ASTM D1876 on polyethylene-laminated paper. Indirect food contact compliance is traceable to FDA 21 CFR §175.105 and §176.170 for packaging of dry and aqueous non-fatty foods, confirmed by overall migration below 10 mg/dm² under EN 1186-1 conditions.

    What makes a one-part VAE suitable for EN 204 D4 wood floor bonding without catalyst pre-mix?

    Durability class D4 per EN 204:2016 requires adhesive films to survive 4 h boiling followed by immediate shear testing, a protocol that destroys conventional vinyl acetate-ethylene dispersions unless a post-applied isocyanate hardener is uniformly mixed on site. DA-142 obviates that two-component process because pendant carboxylic acid groups distributed along the polymer backbone react with latent aluminium chloride hexahydrate (0.6–1.0 phr) already dispersed in the formulation during kettle compounding. The resulting ionic crosslinks densify only when the water phase evaporates and the film pH drops below 5.2, preserving open time on oak staves at 22°C and 55% RH for up to 12 min. Application is performed with a toothed trowel delivering 180–220 g/m² wet adhesive to one face of a planed beech or merbau board. After 60 min closed assembly under 0.5–0.8 MPa clamping pressure and a seven-day conditioned cure at 23 ± 2°C, tensile shear strength measured on 5 mm × 130 mm × 25 mm lap-shear specimens per EN 205 regularly surpasses 10 N/mm² with wood failure exceeding 70%. Production-line data from a continuous radio-frequency edge-gluing press operating at 13.56 MHz show that heating the bond line to 75–85°C within 90 s reduces press-cycle dwell time by 40% compared with cold-set PVA types while still meeting the boil test requirement after 72 h post-conditioning.

    Equipment fouling remains the dominant bottleneck in high-volume D4 assembly: DA-142 exhibits a Brookfield RVT viscosity of 2,000–4,000 mPa·s at 25°C, but shear thinning is limited above 50 s⁻¹, thus forcing the use of positive-displacement piston pumps for recirculation loops rather than lower-cost diaphragm units. Accumulated dried crust on doctor blades must be removed with a pH 9.5 sodium bicarbonate soak every 8 h shift; acetone or ethyl acetate solvents cause irreversible partial coagulation. The wood-adhesive sector also imposes formaldehyde emission ceilings—since DA-142 contains no intentionally added formaldehyde donors, finished assemblies routinely meet ≤0.05 ppm chamber concentration per EN 717-1:2004 without supplemental scavengers.

    If silicate-filled waterproofing slurries exceed 65% solids during high-shear mixing

    Two-component flexible cementitious waterproofing membranes rely on a polymer-to-cement weight ratio between 0.15:1 and 0.25:1 to achieve crack-bridging capability above 0.75 mm at -5°C as defined in GB/T 23445-2009 Type II. When the liquid component is based on DA-142, the dispersion must first be blended with a 0.3 wt% (on total liquid) polycarboxylate superplasticizer using a Cowles blade at 600 rpm before the dry mix—comprising 42.5R ordinary Portland cement, 200-mesh quartz sand, and 2% calcium formate accelerator—is slowly added under agitation. Once combined solids exceed 65%, the torque on a laboratory-scale 1 HP dual-shaft mixer can spike to 8–12 N·m if the VAE dispersion begins to destabilize through calcium-ion shock. Process engineering data indicate that maintaining the emulsion temperature below 30°C and adjusting the powder addition rate to keep the mixer bowl vacuum-assisted at -0.08 MPa eliminates air-entrapped macrovoids that would otherwise reduce the 28-day compressive strength by 8–15%.

    The cured composite, applied by a notched squeegee at 1.5–2.0 kg/m² per coat, develops a continuous interpenetrating network in which DA-142 films line capillary pores with a measured average thickness of 50–120 nm as imaged by cryo-SEM. This microstructure yields a water impermeability index below 0.1 mL/h under 0.3 MPa pressure (JC/T 984-2011) and a chloride diffusion coefficient of less than 5 × 10⁻¹² m²/s per ASTM C1556, making the system suitable for potable-water tank linings after curing for 14 days and passing a 72 h migration test to verify extractable organic carbon stays under 0.5 mg/L.

    Automotive interior PVC vacuum laminating and migration-resistant bond lines

    Vacuum forming of ABS or polypropylene instrument-panel substrates with a 0.8–1.2 mm PVC skin requires a spray-applied adhesive that remains tacky after flash-off yet does not permit plasticizer diffusion from the vinyl compound into the bond plane. DA-142, formulated as a 47% solids ready-to-spray with 3 phr tributoxyethyl phosphate coalescent and 0.2 phr polyether siloxane wetting agent, is deposited at 50–70 g/m² wet via a Kremlin Airmix® gun at 4 bar atomization pressure, targeting a dry film thickness of 22–28 µm. After a 90 s flash-off at 70°C under infrared panels calibrated to 2.5 kW/m² radiant intensity, the coated substrate is transferred into a vacuum membrane press. Cycle parameters—120°C platen temperature, 0.6 bar vacuum for 30 s, followed by 2.5 bar positive pressure for 45 s—activate the VAE film to a surface temperature of 102–108°C, well above its Vicat softening point, ensuring full contour replication on grained PVC.

    The principal failure mechanism in this application is plasticizer-induced creep, which can cause read-through of grain loss after 1,000 h of thermal cycling between -30°C and 80°C per DIN EN 12746. Peel-strength retention on specimens aged in contact with DOP-plasticized PVC commonly falls to 35–40% of initial for uncrosslinked adhesives; DA-142 formulations that incorporate a blocked amine crosslinker activated above 95°C retain 78–85% of initial 180° peel adhesion (ISO 8510-2) after equivalent aging, with the locus of failure shifting from interfacial delamination to cohesive film rupture. A well-controlled line run captures fogging test results (DIN 75201) of below 0.5 mg condensate on gravimetric foils, essential for OEM approval under VDA 278 thermal desorption protocols.

    Random carded web saturation lines operating at 150 m/min demand rapid wetting of fiber surfaces having contact angles that routinely exceed 80° for polyester blends. DA-142 is diluted to 18–22% total solids with deionized water and adjusted to a surface tension of 33–36 mN/m using a nonionic ethoxylate surfactant dosed at 0.15% on bath weight. The web passes through a submerged perforated-roller dip system, followed by a vacuum slot extracting excess liquor to achieve a consistent pickup of 12–16% dry binder on fiber weight. Because medical drapes governed by AAMI PB70:2022 must resist liquid penetration above 20 cm hydrostatic head, a formaldehyde-free crosslinker—ammonium zirconium carbonate at 1.2–1.8% on binder solids—is metered into the bath with a static in-line mixer immediately upstream of the applicator to minimize pot-life issues. The saturated web is dried over a series of steam-heated cans profiled from 110°C to 135°C over 12 s residence, triggering carboxyl-zirconium gelation that elevates wet tensile index to at least 6 N·m/g as measured by ISO 9073-3 after 1 h water immersion. Odor and volatile organic compound residuals remain below 30 µg/g total when tested by headspace GC-MS per VDA 277, a prerequisite for surgical-gown laminates that are sterilized by ethylene oxide.

    Carpet secondary backing adhesion measured against ASTM D3936 delamination thresholds

    Tufted broadloom carpets receive a frothed VAE compound to lock individual yarns before a woven polypropylene secondary backing is attached. The froth is generated by injecting 150–180 mL of air per 100 g of compound through a Hansa Mixer with a 12-pin rotor at 800 rpm, expanding the DA-142 and 40 phr calcium carbonate masterbatch from a density of 1.2 g/cm³ down to 0.55–0.70 g/cm³. The foam must remain open-cell and stable for 3–5 min on the conveyor before the secondary backing is laid down; premature cell drainage concentrates the binder at the backing interface, elevating peel strength to over 35 N/50 mm but inducing a harsh hand and excessive fiber penetration visible through the face yarn. A properly designed formulation for DA-142 uses ammonium stearate at 3.5 phr as the foaming agent, with gelation triggered by heating the web surface to 130°C in the first 20 s of the curing oven.

    Delamination resistance according to ASTM D3936, recorded on specimens conditioned for 24 h at 23°C/50% RH, must fall between 5.5 N and 22 N to satisfy both durability and end-user aesthetics. DA-142 provides a critical control lever through its carboxyl content—raising the aziridine crosslinker addition from 0.5% to 1.5% on binder solids shifts the peel value from 9 N to 18 N while simultaneously reducing wet delamination loss after 24 h water soak to below 20% of the original value, a CRI 105-compliant metric. Production lines that previously ran styrene-butadiene latex often convert to DA-142 to eliminate residual styrene monomer below the 0.5 mg/m³ indoor air emission benchmark without altering the existing pan-and-roll application head or the three-pass 18 m hot-air oven.

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    Certification & Compliance
    More Introduction

    A vinyl acetate-ethylene copolymer dispersion carrying the designation DA-142, manufactured by Dairen Chemical Corporation, represents a medium-solids, carboxyl-functional grade engineered for permanent-pressure-sensitive and laminating adhesive formulations where a balance of cohesive strength, adhesion to low-energy substrates, and plasticizer tolerance is required. Typical physical properties include a solids content of 55 ± 1 % by weight, a Brookfield viscosity (spindle 3, 20 rpm, 25 °C) in the range 2 000–4 000 mPa·s, pH between 4.0 and 5.5, and a minimum film-forming temperature (MFFT) of 0 °C. The dispersed phase exhibits a volume-median particle diameter of approximately 0.5–0.8 µm, and the emulsion is stabilized with a polyvinyl alcohol (PVOH)/surfactant system that introduces the carboxylic acid functionality required for post-crosslinking reactions. Residual vinyl acetate monomer content is maintained below 1 000 ppm under typical production quality control, and the product complies with the compositional requirements of U.S. FDA 21 CFR 175.105 for indirect food-contact adhesives when formulated appropriately.

    Where DA-142 diverges from standard homopolymeric polyvinyl acetate dispersions is in the incorporation of ethylene segments along the copolymer backbone, which permanently internally plasticizes the polymer. This structural feature reduces the need for external coalescing solvents or fugitive plasticizers to achieve film formation at service temperatures approaching freezing. In accelerated migration testing conducted per ASTM D2197 on biaxially oriented polypropylene (BOPP) film, DA-142-based laminating adhesives containing 3–5 phr of a rosin ester tackifier exhibited plasticizer migration values 30–40 % lower than a conventional PVAc homopolymer of equivalent solids after 14 days at 50 °C, a distinction assigned to the reduced free volume of the ethylene-modified chain and its higher molar cohesion energy density.

    Does carboxylation depth determine re-dispersibility limits in high-speed lamination?

    Carboxyl content in DA-142 is specified as an acid number of 2–5 mg KOH/g dry polymer, a deliberately narrow window that balances colloidal stability against premature thickening when ionically crosslinked. On a 250 m/min laminating line equipped with a multi-roll gravure coater, pre-neutralization with ammonium hydroxide to a target pH of 6.8–7.2 generates a viscosity plateau suited for transfer efficiency above 90 % without doctor-blade chatter. However, over-neutralization beyond pH 7.5 induces a rapid yield-stress build-up that manifests as adhesive starve-feed defects, especially when the emulsion is blended with high-acid-number rosin dispersions (acid number > 140). Published data measuring shear viscosity at 100 s⁻¹ on a cone‑plate rheometer (40 mm, 2°) show a 400 % increase in viscosity when the pH drifts from 7.0 to 7.6, attributable to secondary carboxyl-rosin ester exchange reactions rather than simple ionic thickening.

    Operationally, the emulsion must be stored at 5–35 °C; freeze–thaw stability is limited to 2 cycles without protective glycol addition. When used in laminating adhesives for polyethylene terephthalate (PET) to polyethylene foam, the recommended wet-coat weight of 18–22 g/m² (dry) yields a 180° peel strength, tested per ASTM D903 after 72 h conditioning at 23 ± 2 °C and 50 ± 5 % RH, of 4.5–6.0 N/25 mm with cohesive failure observed in the foam substrate above that range.

    Pressure-sensitive adhesive (PSA) tapes prepared with DA-142 require careful selection of tackifier emulsions. Hydrogenated glycerol esters with a Ring & Ball softening point of 85–95 °C and acid number < 6 provide the best loop tack (ASTM D6195) and shear adhesion failure temperature (SAFT) compromise. At 40 wt% tackifier loading on dry binder, the SAFT measured by ASTM D4498 with a 1 kg weight and 25 × 25 mm bond area climbs from 72 °C for a C9 hydrocarbon resin to 94 °C for the hydrogenated rosin ester, while static shear adhesion at 40 °C exceeds 100 h without failure. The inherent VAE backbone, however, imposes an upper service temperature ceiling of approximately 120 °C before thermal discoloration and chain scission accelerate, a boundary not encountered with UV-cured acrylic PSAs.

    Wood-adhesive rheology and bond durability—distinguishing DA-142 from crosslinking PVAc grades

    In cold-press and high-frequency wood assembly, DA-142 occupies a niche between slow-setting, water-resistant PVAc homopolymers (Dincer D3 class per EN 204/205) and more expensive two-component polyurethane dispersions. Unlike D3-type PVAc homopolymers that rely on aluminum chloride or zirconium salt crosslinkers, DA-142 derives a portion of its water resistance from the intrinsic hydrophobicity of the ethylene comonomer and the ability of carboxyl groups to coordinate to multi-valent metal ions when a latent acid-curing catalyst, typically an organic titanate chelate at 1–2 % on wet adhesive weight, is added just before application. On beech wood adherends conditioned to 12 ± 1 % moisture content, adhesive joints cured for 2 h at 20 °C and 0.7 MPa platen pressure develop mean dry shear strengths of 12–14 MPa (ISO 9653), with wood failure percentages exceeding 80 %. After the 4-h boiling-water soak cycle dictated by EN 204 durability class D4, residual shear strength typically falls to 2.5–3.5 MPa, a value sufficient for many interior furniture applications but below the 4 MPa threshold often quoted for D4 classification, indicating that DA-142, even with titanate crosslinking, should be regarded as D3+ rather than a full D4 product unless combined with a melamine-formaldehyde co-binder.

    The emulsion’s compatibility with polyvinyl alcohol extenders and starch fillers is exploited on high-speed paper tube winding lines. At a line speed of 80–120 m/min, a blend consisting of 70 wt% DA-142, 20 wt% calcium carbonate slurry (60 % solids, 2 µm median particle size), and 10 wt% of a 15 % polyvinyl alcohol solution (degree of hydrolysis 88 %, viscosity 20–25 mPa·s at 4 % solids) yields a pick-to-pick bond strength, measured semi-quantitatively by a dedicated peel jig on the winder, that surpasses that of a starch-based control by a factor of 1.8, while maintaining biodegradability profiles acceptable under EN 13432 for compostable packaging when the inorganic filler is replaced with calcium carbonate sourced from paper mill sludge.

    Coating binder formulations—scrub resistance and film coalescence at ambient cure

    Low-odor, solvent-free architectural paints formulated with DA-142 as the primary binder benefit from MFFT depression without the addition of volatile coalescents. In an internal industry study referenced in Dairen’s technical bulletin, a 45 % PVC interior flat paint containing 12 wt% DA-142 (based on total liquid paint) exhibited a wet scrub resistance of 1 200 cycles before failure when tested according to ASTM D2486 method B, a result competitive with vinyl acrylic binders of higher Tg but lower solids. The scrub resistance is sensitive to the type and dosage of associative thickener: a hydrophobically modified ethoxylated urethane (HEUR) thickener at 0.3 wt% active on total paint increased low-shear (0.1 s⁻¹) viscosity to 25 Pa·s while preserving high-shear (10 000 s⁻¹) viscosity at 0.12 Pa·s, a rheology profile matched to a 10 mil bird bar application without roller spatter. Replacement of DA-142 in the same formulation with a standard PVAc homopolymer of +2 °C MFFT required addition of 2 wt% Texanol™ coalescent to achieve equivalent film integrity at 5 °C cure, undermining the VOC-free classification under European Directive 2004/42/CE phase II limits.

    However, the ethylene segments render the polymer film more susceptible to photo-oxidative discoloration compared to pure acrylics. In QUV-B accelerated weathering (ASTM G154, cycle 4: 8 h UV at 60 °C, 4 h condensation at 50 °C), DA-142 clear films develop a Δb yellowness index shift of +4.2 after 500 h, whereas a styrene-acrylic control under identical conditions shows +1.8. Exterior paint systems utilizing DA-142 therefore typically incorporate 0.5–1.0 phr of a hindered amine light stabilizer (HALS) and a benzotriazole UV absorber, extending the time to noticeable yellowing beyond 1 000 h. This requirement is often stated as a formulation caveat in exterior semi-gloss specifications referencing MPI #10 and MPI #15.

    At a nonwoven saturation line—process windows and formaldehyde-free compliance

    Needled polyester and glass-mat nonwovens are saturated with DA-142 by kiss-roll or spray application on machinery running at 30–80 m/min, with wet pick-up controlled between 100–250 % on fabric weight. In air-through ovens operating at 150–170 °C, the emulsion’s low MFFT facilitates rapid film formation before complete water evaporation, minimizing migration of the binder to the mat surface. For a 60 g/m² spunlace polyester mat, a dried binder add-on of 20 ± 2 % imparts a dry tensile strength (MD, ISO 9073-3) of 85–110 N/5 cm versus 32 N/5 cm for the unbonded web. Crucially, DA-142 as a VAE does not release formaldehyde during cure, a property leveraged by manufacturers seeking certification under OEKO-TEX® Standard 100 product class I or GREENGUARD Gold. In contrast, many N-methylolacrylamide (NMA)-functionalized self-crosslinking acrylic binders emit formaldehyde at levels exceeding 16 µg/m³ during simulated chamber testing per EN 717-1, whereas DA-142-saturated felts report non-detectable formaldehyde (< 2 µg/m³) under the same protocol.

    Processing limitations include a sensitivity to mechanical shear in the presence of high-hardness calcium carbonates. In a recirculation loop fitted with an eccentric-cavity pump (200 L tank, 3.0 kW motor), the emulsion maintained particle size stability for 8 h only when the filler grade exhibited a Mohs hardness below 3.5 and the total solids of the mix did not exceed 62 %. Exceeding 65 % solids led to a rise in screen residue on 180 µm mesh to over 2 000 mg/kg within 3 h, a condition that generated streaking defects on the saturated web.

    Comparative Properties of Dairen VAE Emulsions for Adhesive Laminates
    PropertyDA-141DA-142Test Method
    Solids content (%)55 ± 155 ± 1ISO 3251
    Viscosity (mPa·s, 25 °C)1 500–3 0002 000–4 000Brookfield RVT #3, 20 rpm
    pH4.0–5.04.0–5.5ISO 976
    MFFT (°C)+30ASTM D2354
    Carboxyl functionalityNoneYes, acid number 2–5Internal titration
    Plasticizer migration resistance*22 %32 %ASTM D2197, modified
    Re-stick after 4 h at 70 °CModerateHigh, adjusted via crosslinkingInternal loop-tack test

    * Expressed as weight loss of plasticized PVC sheet after contact; lower value indicates better barrier.

    When placed alongside grades such as DA-141, which lacks carboxyl functionality, DA-142 offers post-coatable crosslinking capability that DA-141 cannot match without the addition of external crosslinkers like polyisocyanates. This makes DA-142 the preferred selection for triplex laminates involving aluminum foil-to-paper where heat-seal lacquer demands must be combined with waterborne compliance under FDA 21 CFR 176.170 and 176.180. DA-141, with its slightly higher MFFT and lower plasticizer tolerance, remains more appropriate in bulk paper-to-paper lamination where cost sensitivity and starch compatibility dominate over adhesion to critical substrates. Other Dairen VAE grades, such as DA-1100 with a Tg near −15 °C and solids of 60 %, supply higher tack and elongation but at the cost of lower cohesion, requiring substantial reinforcing by hydrocarbon tackifiers to pass a 50 °C creep test (ASTM D3654, 1 kg/ 25 mm²). The design space of DA-142 therefore targets the mid-range where ambient-temperature cohesion, plasticizer resistance, and ionic crosslinking responsiveness converge without moving to the higher raw-material cost of vinyl acetate-ethylene-vinyl chloride terpolymers or acrylic hybrids.

    On a Berstorff ZE 25 twin-screw extruder (L/D 40) used to compound DA-142 with maleated polyethylene waxes (acid number 25 mg KOH/g, Mw ≈ 8 000) for hot-melt-compatible dispersion powders, the screw speed window is constrained to 180–220 rpm. Below 160 rpm, the wax-rich phase segregates during starved feeding; above 240 rpm, the melt temperature exceeds 115 °C, surpassing the onset of thermal degradation detected by purge gas FTIR as an increase in acetic acid concentration beyond 300 ppm. This narrow processing window contrasts sharply with the broader latitude of ethylene-vinyl acetate (EVA) copolymer grades typically used in hot-melt powder manufacture, underscoring the necessity for temperature-controlled barrel zones and high-precision liquid-injection ports when converting DA-142 to redispersible powder forms.