| HS Code | 215265 |
| Appearance | Milky white liquid |
| Polymer Type | Vinyl acetate ethylene (VAE) copolymer |
| Solid Content | 55 ± 1% |
| Viscosity | 3000 - 5000 cP at 25°C |
| Ph | 4.5 - 6.0 |
| Glass Transition Temperature | Approx. -5°C |
| Minimum Film Forming Temperature | Approx. 0°C |
| Particle Size | 0.5 - 2.0 μm |
| Specific Gravity | 1.05 - 1.07 at 25°C |
| Surface Tension | 35 - 40 dyn/cm |
| Residual Vinyl Acetate Monomer | Less than 0.5% |
| Stabilizer Type | Polyvinyl alcohol (PVOH) |
As an accredited Dairen DA-107 VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dairen DA-107 VAE Emulsion is packaged in 200 kg drums, ready for use in adhesives and coatings. |
| Container Loading (20′ FCL) | 20′ FCL loading of Dairen DA-107 VAE Emulsion: secure drums, prevent shifting, ensure ventilation, avoid extreme temperatures during transit. |
| Shipping | Dairen DA-107 VAE Emulsion ships in sealed drums, IBC totes, or bulk tankers. Protect from freezing, extreme heat, and direct sunlight. Store upright and secure during transit. Not classified as hazardous under standard transport regulations, but avoid spills and ensure proper labeling and documentation. |
| Storage | Store Dairen DA-107 VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Maintain storage temperature between 5°C and 35°C; do not allow freezing. Keep containers off the floor and rotate stock. Use within shelf life, stirring gently before use. |
| Shelf Life | Shelf life is typically 12 months from production date when stored in sealed containers, protected from frost and direct sunlight. |
Solvent-free composite adhesives designed for high-speed flexographic lamination impose a specific set of film-formation constraints: the copolymer must coalesce into a film that resists tunnelling at creases after exposure to −20°C chill-chain transport, yet does not block under 0.3 MPa roll pressure during rewind. DA-107 VAE, with an ethylene-vinyl acetate sequence distribution yielding a glass transition onset near −18°C as measured by modulated DSC at 10 K/min, permits tack development on low-surface-energy substrates without the addition of migratory plasticisers that would compromise indirect food contact status. On production laminators equipped with 200‑line/cm ceramic anilox rolls and three-zone air flotation dryers operating at 75–95–110°C, the emulsion is typically let down with a pressure-sensitive terpene-phenolic tackifier dispersion (5–10 parts wet per 100 parts DA-107 wet) and a hydrophobically modified ethoxylated urethane thickener that sets the low-shear viscosity to 800–1200 mPa·s (Brookfield LV, spindle #3, 12 rpm, 25°C). The gap-adjusted comma bar deposits a wet film that dries to a nominal coat weight of 2.8–4.0 g/m² on 12 μm corona-treated LDPE; a second nip station laminates it to 250 g/m² GC1 clay-coated board. Here, a process conflict emerges: if the drying rate exceeds the copolymer’s minimum film-formation temperature in the first two zones, microcracks appear at the adhesive-board interface, lowering peel strength below 1.2 N/15 mm as per ASTM D903‑98 (180° peel, 300 mm/min). To mitigate this, web temperature is ramped to avoid a dew-point condensation shock when the coated film enters zone one, and relative humidity at the coater head is held below 55% to prevent skinning on the gravure cells. The finished laminate conforms to FDA 21 CFR 175.105 and EU Regulation 10/2011 overall migration limits (simulant D2, 40°C, 10 days) and is converted into snack food pouches, outer carton lamination for frozen seafood, and stand-up dry-goods bags with press-to-close zippers. Batch-to-batch variance in DA-107’s mean particle diameter—typically 0.8–1.2 µm—has been observed on 50‑line laser diffraction to shift the tackifier demand by up to 3 phr, a sensitivity that requires incoming material testing before each bulk blending cycle.
Nonwoven producers converting flash-dried cellulose pulp into airlaid webs for household and baby wipes rely on the binder to deliver an instantaneous wet burst reinforcement that survives a saturated soak at pH 5.5 without fibre debonding. DA-107 is sprayed as a dilute aqueous formulation (2–5% dry solids addition on fibre weight) through an array of low-pressure hydraulic nozzles operating at 3–5 bar onto the moving formed web, immediately upstream of a through-air drum dryer that raises the web temperature to 135°C in 18–22 seconds. The addition ratio is calibrated so that the copolymer constitutes 90–95% of the binder solids, the remainder being a fugitive wetting aid—commonly an alcohol ethoxylate with an HLB of 11–13—that evaporates during curing and does not contribute measurable volatile organic compound residues above the 0.5 mg/m² threshold. Swelling trials on an Instron model 3345 equipped with a 1 kN load cell according to EDANA NWSP 110.5.R0 show that the wet MD tensile index reaches 2.8–3.5 N·m/g when the copolymer’s ethylene segments create hydrophobic domains that restrict water wicking into the fibre joint, while the vinyl acetate blocks simultaneously preserve adhesion to the cellulose hydroxyl sites. Compliance is anchored to ISO 10993‑5:2009 for cytotoxicity (L929 mouse fibroblast cell line, 48 h extract) and OEKO-TEX Standard 100 Annex 4 product class I requirements, with reduction of formaldehyde donors and crosslinkers that can elicit skin sensitisation in neonate end-users. The final roll goods—with basis weights of 35–65 g/m²—are converted into wet-laid mopping cloths, flushable dispersible wipes, and biodegradable personal care sheets that meet EDANA flushability guidelines.
In carpet back-coating operations where line stops longer than 90 seconds cause premature skinning on the kiss-coater rolls, the rheological stability of DA-107 at low shear rates becomes a critical parameter. The pre-coat compound is formulated by charging a 1000 L pneumatic ribbon blender with DA-107 (35–42% of the wet compound), ground calcium carbonate filler (median particle size 12 µm, loaded at 400–600 parts per 100 parts dry emulsion), a sodium polyacrylate dispersant (0.15 parts dry), and a wax emulsion (2–3 parts dry) to improve scuff resistance. After 20 minutes of low-speed mixing under 0.5 bar vacuum to remove entrained air, the compound is pumped to an air-knife applicator that meters a wet coat weight of 550–700 g/m² onto polypropylene primary backing. A three-pass air impingement oven with residence time of 2.5–3.5 minutes provides the energy to raise the film temperature to 115°C, at which point the copolymer interdiffuses into the tufted yarn bundles. The dried pre-coat must achieve a tuft bind strength exceeding 3.5 N per ASTM D1335‑21 (cut loop specimen, gauge length 76 mm, constant rate of extension 300 mm/min) to prevent fuzzing during the secondary backing lamination that follows immediately. Because calcium stearate migration from the filler can reduce interfacial adhesion by 15–20% after 6 months of warehousing, the formulation includes 0.2 wt% of a hydrophobic fumed silica to stabilise the bond. The end product is a fully adhered unitary carpet tile for high-traffic office environments, emission-tested according to CRI Green Label Plus using ASTM D5116‑17 small-chamber protocols, with total VOC emission after 24 h below 0.5 mg/m³.
One-component, moisture-curing construction sealants formulated with DA-107 as the polymeric base compete with silicones in low-movement floor and drywall joints by eliminating acetic-acid odour and paint-contamination issues. The formulation is processed in a planetary double‑Z mixer under full vacuum (−0.095 MPa) and comprises DA-107 at 30–38 wt%, di‑isononyl phthalate plasticiser (15–20 wt%), precipitated calcium carbonate filler (40–45 wt%), benzophenone UV absorber (0.2 wt%), hindered amine light stabiliser (0.1 wt%), and a silane‑terminated polyether moisture scavenger added at 1.5–2.5 wt% to drive the tack-free time to 12–18 minutes at 23°C/50% RH. The material is filled into 300 mL aluminium cartridges and extruded through a 6×12 mm rectangular nozzle onto lightly sanded concrete; the elastic recovery measured per ISO 7389:2002 after 100% extension must exceed 70% to satisfy designation 25LM under ISO 11600:2011. A cycle of 1000 h QUV‑A accelerated ageing (ASTM G154‑23, cycle 1, irradiance 0.89 W/m² at 340 nm) results in a surface Shore A shift of less than +5 units, an outcome only possible when the UV absorber/hindered amine stabiliser pair is pre-dispersed in the plasticiser before powder addition, otherwise surface chalking initiates within the first 200 h. The cured sealant bead holds a tensile strength at break of 0.45–0.6 MPa per ISO 37:2017 Type 2 dumbbell, and is specified for residential expansion joints up to 12 mm width and drywall perimeter seals where VOC content stays under 50 g/L per EU Directive 2004/42/EC subcategory A/g.
Unlike two-component polyurethanes, the one-part VAE dispersion employed for D3 wood adhesives eliminates exothermic cure risks during large-volume batch mixing in a continuous laminating plant for window scantlings. The base adhesive is supplied at 55% solids and is blended with a hydrophobic fumed silica (1.5–2.5 parts per 100 parts wet DA-107) to impart sag resistance on vertical finger joints. Immediately before the glue is fed to a roller coater, an aliphatic isocyanate crosslinker with an NCO content of 22% is metered in at 3.5–4.5 wt% of the wet adhesive weight, initiating a latent crosslinking reaction that cuts the cold‑pressing time from 18 minutes to 8 minutes at 0.6 MPa clamp pressure. The laminate, consisting of three plies of 20 mm spruce, is subsequently aged for 7 days at 20°C/65% RH before being subjected to the EN 204:2016 D3 sequential immersion test (4 days water soak at 20°C followed by 7 days standard climate). A minimum shear strength of 2.0 MPa with wood failure percentage greater than 80% must be retained; DA-107-based formulations consistently exceed this threshold provided that the moisture content of the adherends is maintained between 10–14% and that the freshly machined surfaces are assembled within 45 minutes to avoid extractive migration. The finished product is a finger-jointed laminated core for interior timber windows, free of formaldehyde and labelled according to EN 14080:2013.
A transfer coating line applying DA-107 as a permanent-tack label adhesive onto a 36 µm biaxially oriented polypropylene facestock requires a coating weight precision of ±0.3 g/m² to keep the loop tack within the 4–6 N/25 mm sweet spot for semi‑removable price marking. The emulsion is thickened with a hydrophobically modified alkali‑swellable emulsion (0.3–0.5 dry phr) to a steady‑shear viscosity of 2500–3500 mPa·s at 50 s⁻¹ and applied via a slot‑die coater onto a silicone‑release PET liner running at 35 m/min. The two‑zone air flotation dryer profile is set to 65–105°C such that the web surface temperature remains below 95°C; exceeding 105°C causes the silicone crosslink network to degrade and transfer silicone to the adhesive, collapsing 180° peel adhesion on glass below 1.0 N/25 mm. After the adhesive film reaches its target dry coat weight of 20–22 g/m², a corona‑treated BOPP facestock is laminated in‑line under a rubber‑covered nip at 40 N/cm line pressure. The pressure‑sensitive laminate is slit and die‑cut into label rolls whose adhesive side must pass FDA 21 CFR 175.125 for incidental contact with whole fruit under room‑temperature shelf conditions. During summer campaigns when ambient humidity exceeds 75%, a pre‑drying step for the silicone liner is introduced to avoid blister formation at the transfer nip; otherwise micro‑delamination stripes become visible after 72 h curing. Long‑term removability is verified via FINAT test method FTM 1 after 90‑day dwell on painted steel panels, requiring clean peel with adhesive residue below 2% of the label area.
| Application | Standard | Key Clauses / Test Methods | Mandatory Requirement |
|---|---|---|---|
| Flexible packaging laminating adhesive | FDA 21 CFR 175.105 | Indirect food additive – adhesives; overall migration to food simulants per EU 10/2011 | No detectable transfer above 10 mg/dm² (simulant D2) |
| Hygienic nonwoven binder | OEKO-TEX Standard 100, ISO 10993‑5:2009 | Annex 4, product class I; L929 cytotoxicity assay, 48 h extract | No cell lysis; general toxicity score = 0 |
| Carpet pre-coat compound | CRI Green Label Plus | ASTM D5116‑17 small-chamber emission test; TVOC after 24 h | TVOC ≤ 0.5 mg/m³ |
| Construction joint sealant | ISO 11600:2011 | Class 25LM; elastic recovery ≥ 70% per ISO 7389 | Movement accommodation factor 12.5% |
| Wood adhesive (D3 durability) | EN 204:2016 | D3 sequential immersion; shear strength after 4-day soak | ≥ 2.0 MPa with wood failure > 80% |
| Removable label PSA | FDA 21 CFR 175.125 | Pressure-sensitive adhesives for food contact; FINAT FTM 1 | Clean peel after 90‑day dwell; residue < 2% label area |
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| Parameter | DA‑107 VAE | PVAc homopolymer (D3) | Styrene-acrylic copolymer (D4) |
|---|---|---|---|
| MFFT ( °C) | 0 | +6 to +10 | +12 to +25 |
| Coalescent demand at 5 °C application | none | 5 % – 8 % on binder solids | 8 % – 12 % on binder solids |
| Creep resistance EN 14257 (WATT 91) | 0.2 – 0.5 mm after 24 h/80 °C | 1.8 – 3.2 mm | 0.8 – 1.5 mm |
| Plasticizer migration into polystyrene foam | absent (intrinsic flexibilization) | dibutyl phthalate migrates within 72 h | absent |
| Heat reactivation at 60 °C | full (>85% of original shear strength) | partial (<40%) | negligible |
| Component | Low‑cost blend (wt%) | D3 pass (wt%) | Fast‑setting variant (wt%) |
|---|---|---|---|
| DA‑107 VAE (as received) | 92.0 | 88.5 | 85.0 |
| Polyvinyl alcohol (10% solution, 88 mol% hydrolysis) | 3.0 | 5.0 | — |
| Calcium carbonate (10 µm, coated) | 5.0 | 5.0 | 10.0 |
| Aluminium chloride (30% solution in water) | — | 1.5 | 5.0 |
| Defoamer (mineral oil‑based) | 0.2 | 0.2 | 0.2 |
| Preservative (isothiazolinone combination) | 0.1 | 0.1 | 0.1 |
| Water | balance to 100 | balance to 100 | balance to 100 |