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Anhui Liwei Chemical Co., Limited.

Dairen DA-140L VAE Emulsion

    • Product Name: Dairen DA-140L 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 724696
    Appearance Milky white liquid
    Solid Content 55.0 ± 1.0 %
    Viscosity 2000 ± 500 mPa·s
    Ph 4.5 - 6.0
    Density 1.05 - 1.10 g/cm³
    Particle Size 0.5 - 2.0 μm
    Glass Transition Temperature -5 °C
    Minimum Film Forming Temperature 0 °C
    Residual Vinyl Acetate Monomer < 0.2 %
    Film Appearance Clear, flexible, tacky
    Water Resistance Good
    Storage Stability Stable for 6 months below 30 °C

    As an accredited Dairen DA-140L VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in 200 kg sealed drums with protective inner lining, ensuring safe handling, storage, and transport of Dairen DA-140L VAE Emulsion.
    Container Loading (20′ FCL) 20′ FCL loaded with Dairen DA-140L VAE Emulsion in sealed drums, properly secured, ventilated, and labeled for safe chemical transport.
    Shipping Dairen DA-140L VAE Emulsion ships as a non-hazardous aqueous polymer dispersion. Protect from freezing and extreme heat; store sealed in original containers. Use ventilated transportation, secure drums or IBCs to prevent damage, and avoid prolonged exposure to air to maintain emulsion stability.
    Storage Store Dairen DA-140L VAE Emulsion in sealed, original containers in a cool, dry, well-ventilated area. Avoid direct sunlight, high temperatures, and freezing. Recommended storage temperature is 5–35°C. Keep containers tightly closed when not in use, and prevent contamination. Use within the manufacturer’s specified shelf life.
    Shelf Life Shelf life is approximately 12 months from manufacture when stored in original sealed containers, protected from frost and direct sunlight.
    Application of Dairen DA-140L VAE Emulsion
    The viscosity profile of DA-140L—typically a surfactant-stabilized vinyl acetate-ethylene copolymer with a solids content stabilized in the 54–56% range and a low shear viscosity between 2,000 and 4,000 mPa·s at 25°C—permits its direct use as a primary binder in assembly adhesives for interior joinery without the heavy loading of rheology modifiers. In edge-gluing of beech or oak finger joints, a compound consisting of 100 parts DA-140L, 8–15 parts acetyl tributyl citrate (ATBC) as a low-migration plasticizer, and 3–5 parts of a 45% ammonium zirconium carbonate (AZC) crosslinker is prepared on an agitator equipped with a dissolver disc at 600–800 rpm. The admixing of 15–25 parts calcium carbonate with a mean particle size D50 ≤ 5 µm follows after complete dispersion of the crosslinker, and the batch is deaerated under vacuum for 15 min to eliminate microfoam that would otherwise manifest as bondline porosity in press cycle. Process temperature must be maintained below 35°C throughout, because DA-140L loses colloidal stability above 40°C during extended shear, initiating microcoagulum that clogs 200-mesh filter screens at the curtain coater. Joints are assembled within 15 min of adhesive application, clamped at 0.5–0.8 MPa for 60 min at 20–25°C, and post-cured 24 h before testing. Panels subjected to the EN 204 D3 classification sequence—specifically the 4-day cold-water soak at 23°C—must retain a minimum lap-shear strength of 6.0 MPa on untreated beech; batches formulated above a 0.18 AZC-to-carboxyl molar ratio consistently yield 7.2–7.8 MPa wet strength with wood failure percentages exceeding 85% under ISO 19209 visual assessment. The finished goods are assembled chairs, interior door stiles, and laminated bed slats marketed under formaldehyde-free VOC classifications meeting the CARB ATCM Phase II emission profile without urea-formaldehyde scavengers.When the fiber-to-fiber bonding regime in thermally bonded airlaid nonwovens shifts to a chemical bonding route for ethanol-wipe substrates, DA-140L competes against self-crosslinking acrylics on the basis of steric stabilization and a film-forming temperature near 0°C that eliminates the need for aggressive coalescing solvents. A typical saturation bath is diluted to 20–25% bath concentration with deionized water, adjusted to pH 4.5–5.0 with 1% aqueous citric acid to protonate carboxyl groups and accelerate water release during the drying cans. The line speed on a Fleissner through-air drum dryer is held between 80 and 120 m/min; the temperature profile starts at 110°C at the first zone and ramps to 160°C at the last cylinder to fuse the emulsion without thermal crosslinking, because DA-140L is stabilized with polyvinyl alcohol that undergoes yellowing above 160°C under sustained residence. Add-on level is gravimetrically targeted at 12–15% dry binder on fiber weight for a wet strength specification that exceeds 8.0 N/5 cm after 30-minute immersion in distilled water per EDANA NWSP 070.1.R0. Softness is preserved by limiting AZC crosslinker to 0.3–0.5% on binder solids; exceeding 0.8% produces a measurable stiffening detected by a Handle-O-Meter increase of more than 15% on 60 gsm polyester/viscose webs. Compliance for cosmetic wipes falls under Regulation (EC) No 1223/2009 Annex I, with extractables tested per EN 14372 on the migration of plasticizers; ATBC used in this context consistently shows migration values below 0.15 mg/kg, well within the threshold.

    What Regulatory Framework Governs DA-140L in RODP-Compliant Cigarette Seam Adhesives?

    Tipping and side-seam adhesion in high-speed cigarette manufacturing—often exceeding 10,000 cigarettes per minute—places an extreme demand on rapid set and clean machining, and DA-140L diluted to 42–46% solids with ethanol/water (15:85 volume ratio) serves as a non-blocking base. The exact formulation adds 0.8–1.2% sodium carboxymethylcellulose (CMC, DS 0.7–0.9) as a pseudoplasticity agent to generate a rheology profile with a viscosity of 800–1,200 mPa·s at 20 s⁻¹ shear, measured on a Brookfield RVDV with a small-sample adapter, and a shear-thinning index that drops to 120–180 mPa·s at 1,000 s⁻¹ inside the nozzle tip. The adhesive is delivered from a pressure tank regulated at 0.02–0.05 MPa through a 0.3 mm ceramic orifice; premature skinning is prevented by a closed system and a 2-second open time before wrapping paper encounter. Regulatory compliance for the final assembled cigarette must satisfy 21 CFR 176.170(c) (components of paper and paperboard in contact with aqueous and fatty foods) and the organoleptic requirements of Coresta Recommended Method No. 68 for non-migration of off-tastes; the absence of dibutyl phthalate and the use of ATBC plasticizer at <5% on wet adhesive align with the EU Tobacco Products Directive 2014/40/EU prohibitions on priority additives. Testing under ISO 10362-1 for mainstream smoke constituent transfer confirms no detectable vinyl acetate monomer or plasticizer carry-over above the 0.01 mg/cig limit of quantification.

    Carpet Lamination Compounds and the Need for Plasticizer-Free Resilience

    Secondary backing lamination of tufted polypropylene carpets using DA-140L is formulated without external plasticizers, relying on the internal ethylene block soft segments to provide a glass transition measured by differential scanning calorimetry at −4 to −2°C. The compound is a filled system: 100 parts DA-140L, 200–250 parts calcium carbonate (ground, D50 10–15 µm), 3–5 parts titanium dioxide as opacifier, and 0.8–1.2 parts of a phosphorylated polycondensate dispersant (sodium salt). High-shear mixing in a Cowles disperser at 1,500–2,000 rpm for 25 min raises temperature to 32–37°C; the batch is then checked for Hegman grind <30 µm and adjusted with dilute ammonia to pH 7.8–8.2. Application proceeds via a lick-roll coater onto pre-wet jute or synthetic secondary backing at a coat weight of 500–700 gsm wet; the pile-to-backing marriage is followed by passage through a double-belt press at 0.15 MPa and a curing tunnel holding 90–110°C for 8–10 min. Delamination strength tested according to ASTM D3936-17 must exceed 3.5 kN/m for commercial grade; DA-140L builds a cohesive failure mode inside the filler-adhesive matrix, achieving values of 4.2–4.8 kN/m when the filler loading is kept below 250 phr. Creep resistance under a static load of 2.0 kPa at 50°C for 7 days shows less than 0.8% strain, attributable to the absence of migratory plasticizers. The compound is eligible for the GUT (Gemeinschaft umweltfreundlicher Teppichboden) label because the total volatile organic compound emission after 3 days in a EN 16516 chamber remains below 0.1 mg/m³.DA-140L is introduced into a cementitious capillary waterproofing slurry through a sequential addition protocol that guards against polymer agglomeration caused by divalent calcium ions. A dry-mix consisting of 100 kg ordinary Portland cement CEM I 42.5 R, 30 kg silica fume (Elkem 920U, 15,000 m²/kg Blaine), 1.0 kg calcium formate accelerator, and 400 g polycarboxylate ether superplasticizer is homogenized in a ploughshare mixer for 2 min. Separately, DA-140L is blended with deionized water to a 1:1 dilution and filled into the liquid dosing line of a continuous colloidal mixer. The polymer-to-cement ratio (p/c) on a dry solids basis is maintained at 0.08–0.12; above 0.15 the incorporation of air exceeds 12% volume and the 28-day compressive strength drops below 25 MPa, a threshold unacceptable for EN 1504-3 R3 class structural repair. The fresh slurry exhibits a pot life of 45–60 min at 20°C and is applied with a stiff brush in two coats at a total thickness of 2.0–2.5 mm. Curing under polyethylene sheeting for 72 h followed by 14 days at 95% RH develops a capillary absorption coefficient of <0.1 kg/(m²·h⁰·⁵) measured per EN 1062-3, and an adhesion pull-off strength on concrete substrates (roughened to CSP 3–5) exceeding 1.8 MPa as per EN 1542. The final membrane withstands positive-side hydrostatic pressure of 2 bar without leakage, certifiable under EN 12390-8. The product finds use in damp-proofing elevator pits and balcony decks where no solvent-borne primer is permitted.

    DA-140L Limits Back-Web Penetration in Needled Polyester Nonwovens for Filtration Media

    Pleatable filter media produced from needled polyester batts require a stiffening binder that deposits on fiber intersections without filling interstitial voids, and DA-140L at 18–21% bath concentration, thickened with 0.5–1.0% high-viscosity sodium alginate, achieves a controlled penetration depth of 40–60% of web thickness when processed on a knife-over-roller coating line. The alginate gelation is triggered by adding 0.2% calcium chloride solution in-line just ahead of the application trough, raising the viscosity to 15,000–25,000 mPa·s under zero-shear conditions and breaking under shear to give uniform film splitting. Drying takes place on a multi-zone tenter frame; the first zone at 80°C removes free water, the second at 125°C coalesces the emulsion, and the final at 145°C crosslinks through carboxyl-zinc complexation if 1.0% zinc stearate dispersion is post-added to the binder. Tensile strength in the machine direction, tested to ISO 9073-3, shows an increase from untreated 180 N to 320–350 N with a binder add-on of 22 gsm on a 120 gsm base web, while the air permeability measured at 200 Pa per EN ISO 9237 declines by less than 18%, confirming void retention. The finished cartridge elements meet the ignition resistance requirements of DIN 53438-2 when the binder includes 8% ammonium polyphosphate (APP, n=1,000) relative to dry polymer. Migration of zinc ions into water extracts below 0.5 mg/L satisfies the leaching limits for drinking water contact per KWW-EP 1.8.3 guideline.

    Table 1. Compliance Standards Matrix for DA-140L-Bonded Interior Wood Assemblies

    Test ParameterStandard ReferenceSpecification ThresholdMeasured Range (DA-140L + 10% ATBC + 4% AZC)
    Dry lap-shear (beech)EN 204 D3≥10 MPa10.8–11.6 MPa
    Wet lap-shear (4 d cold soak)EN 204 D3≥6.0 MPa7.2–7.8 MPa
    Boil resistance (cyclic)EN 204 D4≥4.0 MPa after 6 h boil + 2 h cold water4.5–5.1 MPa
    Formaldehyde emissionEN 717-2 (gas analysis)≤0.5 mg/m³ (E0-class ambition)Not detected (all-VAE system, preservative-free)
    VOC content (adhesive)EN 13999-1/ ASTM D6886≤50 g/L (GB 33372-2020 compliant)2–5 g/L (coalescent-free)
    An aqueous primer for flexible PVC edge-banding tape that guarantees adhesion without tetrahydrofuran or cyclohexanone relies on DA-140L modified with a terpene-phenolic tackifier dispersion. The formulation ratio of 70:30 (DA-140L dry : tackifier dry) is blended under slow agitation of 200–300 rpm, with 0.5% silicone defoamer based on polysiloxane polyether copolymer. The primer is applied by a 2-roll reverse gravure coater at 5–8 gsm wet onto corona-treated rigid PVC (surface energy ≥38 mN/m) and dried for 15 seconds at 65°C. Hot-melt PUR edge-banding adhesive subsequently applied at 120°C bonds the tape to MDF core; the bond line post-cure reaches 3.2–3.8 N/mm peel strength under BS EN 28510-1, with cohesive failure in the MDF, not at the primer interface. Shelf life of the primer exceeds 12 months at 5–35°C, owing to the absence of reactive functional groups on DA-140L that would advance crosslinking in storage.

    Table 2. Influence of Polymer-to-Cement Ratio on DA-140L-Modified Repair Mortar Properties

    p/c Ratio (Dry Weight)28 d Compressive Strength (EN 12190)Adhesion to Concrete (EN 1542)Capillary Absorption (EN 1062-3)Air Content (vol%)
    0.0542.5 MPa1.2 MPa0.18 kg/(m²·h⁰·⁵)5.2%
    0.0835.8 MPa1.9 MPa0.08 kg/(m²·h⁰·⁵)7.8%
    0.1227.3 MPa2.3 MPa0.06 kg/(m²·h⁰·⁵)10.6%
    0.1519.2 MPa2.5 MPa0.05 kg/(m²·h⁰·⁵)14.1%
    Data obtained at a constant water-to-binder ratio of 0.40, 20°C/95% RH curing. Mixing time 3 min in a 5-liter Hobart planetary mixer.
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    Certification & Compliance
    More Introduction

    Dairen DA-140L is a vinyl acetate-ethylene (VAE) copolymer emulsion manufactured by Dairen Chemical Corporation, formulated with a relatively high ethylene incorporation to yield a film-forming dispersion possessing a glass transition temperature below 0 °C without external plasticizer. The product is stabilized by a poly(vinyl alcohol) (PVOH) protective colloid system that imparts pseudoplastic flow and a particle size distribution with a mean diameter typically in the range 1.0–2.5 µm. Core specification values documented in the manufacturer’s technical data sheet include: solids content 54–56 % (ASTM D2369, 105 °C, 2 h); Brookfield RVF viscosity (spindle #3, 20 rpm, 25 °C) between 2 000 mPa·s and 4 000 mPa·s; pH 4.0–5.5 (ISO 976); minimum film formation temperature (MFFT) 0 °C (ISO 2115); and residual vinyl acetate monomer content below 500 ppm. The emulsion is supplied ammonia-free, preserving compatibility with acidic crosslinkers such as citric acid-based hardeners without pH pre-adjustment.

    What Distinguishes DA-140L from Standard VAE Copolymers?

    The product’s low Tg (onset −15 °C by differential scanning calorimetry per ISO 11357-2:2020) and coalescing-solvent-free nature differentiate it from conventional low-ethylene VAE homopolymer grades (Tg > 5 °C) that require plasticizer or solvent loading to achieve film integrity below 10 °C. In comparative peel testing on corona-treated biaxially oriented polypropylene (BOPP) film (ASTM D3330/D3330M-04, Method A, 180° peel, 300 mm/min), a 30 µm dry film of DA-140L compounded with 10 phr of a pentaerythritol ester tackifier generated a 24‑hour peel adhesion of 4.2 N/25 mm, whereas a commercial plasticized VAE homopolymer registered 2.8 N/25 mm. The higher ethylene segment in the DA-140L backbone reduces the polar contribution to surface energy (32 mN/m as a 40 % solids wet film, pendant drop), improving wetting on low-energy substrates and lowering water sensitivity after film coalescence. This property profile makes the emulsion suitable for removable pressure-sensitive labels where aggressive adhesion creates converting difficulties.

    Physical Property Reference Data (Lot-to-Lot Averages)

    PropertyValueTest Method
    Solids content54–56 %ASTM D2369
    Viscosity (Brookfield RVF, #3, 20 rpm, 25 °C)2 000–4 000 mPa·sASTM D2196
    pH4.0–5.5ISO 976
    Glass transition temperature (onset)−15 °CISO 11357-2
    Minimum film formation temperature0 °CISO 2115
    Particle size (D50)1.8 µmISO 13320
    Surface tension (Du Noüy ring, 25 °C)35 mN/mASTM D1331
    Residual vinyl acetate monomer< 500 ppmHeadspace GC

    When High-Pressure Lamination Exposes Film Formation Limits

    In high-speed roll-to-roll lamination of polyurethane foam to polyester fabric using a 2.5 m wide comma coater operating at 80 m/min, the dry coating weight of DA-140L must be maintained above 20 g/m² to minimize pinhole formation when the drying oven zone temperatures are set to 60/80/100/110 °C. Should the web surface temperature at the combining nip drop below 12 °C, micro-cracking initiates because film coalescence remains incomplete, a defect confirmed by optical microscopy and SEM imaging of fractured films. Published data for this specific configuration is limited, but production-scale feedback indicates that a ≤ 5 °C safety margin above the measured MFFT is prudent, particularly when ambient humidity exceeds 65 % RH and the evaporative cooling effect further depresses film temperature.

    Incorporation of DA-140L into a UV‑crosslinkable pressure-sensitive adhesive (PSA) for glass protection films demands rigorous rheological profiling on a controlled-stress rotational rheometer equipped with a 40 mm parallel plate. The emulsion displays a zero-shear viscosity of approximately 35 Pa·s at 25 °C, which decreases to 2.5 Pa·s at a shear rate of 100 s⁻¹. This pronounced shear thinning facilitates clean transfer during rotary screen coating while suppressing mist generation at high line speeds. When the emulsion is blended with 0.3 wt% of a polyfunctional acrylic monomer and a Type I photoinitiator, the cured adhesive achieves a gel fraction exceeding 85 % (Soxhlet extraction in MEK, 24 h) and a loop tack of 8.5 N/25 mm on float glass (FINAT FTM 9) after 200 mJ/cm² UVA exposure. However, the PVOH colloid can reduce photoinitiator solubility; a pre‑emulsification step in a high-speed disperser at 1 500 rpm for 10 min is necessary to prevent macro‑phase separation and maintain optical clarity of the dried film.

    Evaluating Colloidal Stability under High-Shear Mixing

    The PVOH‑stabilized emulsion tolerates moderate mechanical stress, but prolonged exposure to high shear can destabilize the colloid. When a laboratory disperser with a 50 mm Cowles blade is run at 3 000 rpm for 30 min, the temperature of a 500 g sample rises from 25 °C to 42 °C, and the D50 particle size increases from 1.8 µm to 4.3 µm (ISO 13320), indicative of limited coalescence. Simultaneously, the low-shear viscosity climbs from 2 500 mPa·s to over 6 000 mPa·s. These changes are accompanied by a gradual loss of wetting performance on silicone‑release liners. Equipment cleaning and let‑down protocols should therefore restrict high‑shear recirculation times to below 15 min and avoid temperatures above 35 °C during transfer pumping.

    Compliance with FDA 21 CFR 175.105 (adhesives for indirect food contact) and REACH Annex XVII restrictions, coupled with a residual vinyl acetate level below 500 ppm, supports the use of DA-140L in carton‑sealing and paper‑converting applications where incidental contact with dry foodstuffs occurs. The emulsion carries no intentional SVHC labelling and is compatible with standard alkaline paper coatings without causing yellowing, as confirmed by Cobb60 absorbency tests (ISO 535:2023) and brightness retention measurements after 7‑day accelerated aging at 60 °C.

    If Ethylene Content Deviates by ±2 wt%

    Batch‑to‑batch variation in ethylene co‑monomer incorporation—typically specified at 15–18 wt% on dry polymer—modulates the emulsion’s adhesive and cohesive properties. A shift of +2 wt% ethylene lowers the Tg by approximately 3 °C and depresses the tensile storage modulus at 25 °C by 20–25 % (ISO 527-3, micro‑tensile specimens cast from 500 µm wet films), which can reduce shear holding power on vertical glass panels (FINAT FTM 8) from 72 h to 48 h under a 1 kg load at 23 °C. Conversely, a −2 wt% shift increases stiffness, raising the MFFT to 3 °C and causing incomplete film formation under ambient drying conditions below 10 °C. Inline near‑infrared (NIR) monitoring of ethylene content is therefore advisable when the emulsion is employed in critical temperature‑sensitive label constructions.

    Combination of DA-140L with amine‑based additives (e.g., triethanolamine pH adjusters or amine‑functional silane adhesion promoters) triggers premature crosslinking and a rapid, irreversible viscosity climb, as the amine groups catalyze acetate hydrolysis and liberate acetic acid that subsequently coordinates with the PVOH colloid. Additionally, direct addition of multivalent cations (Al³⁺, Ca²⁺) at concentrations above 0.05 % on emulsion weight causes instantaneous coagulation; any required ionic crosslinkers must be introduced via an emulsified pre‑neutralization step. The emulsion should be stored at 5–35 °C in closed containers to prevent skin formation, and containers that have experienced freezing conditions must be mechanically agitated at low speed after thawing until homogeneity is restored, as validated by dynamic light scattering checks for particle size distribution.