| HS Code | 555849 |
| Product Name | VINNAPAS 5043 N |
| Chemical Family | Vinyl acetate-ethylene copolymer |
| Product Form | Aqueous dispersion |
| Appearance | Milky white liquid |
| Solids Content | Approx. 52% |
| Viscosity | Approx. 3,500 - 6,500 mPa·s |
| Ph | Approx. 4.0 - 5.5 |
| Glass Transition Temperature | Approx. -15°C |
| Minimum Film Forming Temperature | Approx. 0°C |
| Particle Size | Approx. 0.3 - 1.0 µm |
| Density | Approx. 1.06 g/cm³ |
| Protective Colloid | Polyvinyl alcohol |
| Film Properties | Flexible and clear film |
As an accredited VINNAPAS 5043 N factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | VINNAPAS 5043 N is a VAE copolymer dispersion supplied in 200 kg drums, 1,000 kg IBCs, or bulk tankers. |
| Container Loading (20′ FCL) | VINNAPAS 5043 N is loaded as a 20′ FCL in drums or IBCs, securely palletized and labeled for safe transport. |
| Shipping | VINNAPAS 5043 N is a non-hazardous aqueous vinyl acetate-ethylene copolymer dispersion. Ship as a stable liquid in drums, IBCs, or tank containers. Not regulated as dangerous goods under ADR, IMDG, or IATA. Protect from freezing and temperatures above 30°C, and prevent leakage during transport. |
| Storage | Store VINNAPAS 5043 N in tightly sealed original containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Recommended storage temperature: 5–30°C. Protect from frost, as freezing damages the dispersion. Keep containers closed when not in use and follow shelf-life guidelines before use. |
| Shelf Life | Shelf life is typically 6 months from date of manufacture when stored in original sealed containers at temperatures between 5-30°C. |
VINNAPAS 5043 N is a polyvinyl alcohol-stabilized vinyl acetate-ethylene copolymer dispersion supplied at a nominal solids content of 55%, a Brookfield viscosity range of 4000–8000 mPa·s at 25°C under ISO 2555, and a minimum film-forming temperature near 0°C. The following application sections are limited to production scenarios in which the dispersion functions as the primary colloidal binder or co-binder in adhesives and laminating compounds. Each section records the applicable compliance framework, the addition ratio ranges observed in industrial batch records, the manufacturing process equipment, and the terminal article type. Storage conditions between 5°C and 30°C are assumed; frozen material is excluded from processing because freeze-thaw cycles irreversibly coagulate the dispersion.
| Application segment | Compliance standard or test method | Addition ratio of VINNAPAS 5043 N | Terminal converted article |
|---|---|---|---|
| D3 wood assembly | EN 204:2016 D3; EN 205:2016 | 75–90 wt% of liquid adhesive | Interior joinery, furniture joints |
| Paper-to-film lamination | FDA 21 CFR 175.105; Regulation (EU) No 10/2011 | 45–70 wt% of coating liquid | Dry-food pouches, paper-to-film sachets |
| Spiral paper core winding | ISO 11093-9 | 60–85 wt% of applied adhesive | Paper cores for film and flexible packaging reels |
| Membrane press lamination | EN 311:2005; EN 13986 | 50–80 wt% of formulated adhesive | Cabinet doors, drawer fascias, PVC-wrapped profiles |
| Book casing | REACH 1907/2006/EC; RoHS 2011/65/EU | 70–90 wt% of casing-in adhesive | Hardcover books, reinforced folders |
Wood assembly lines that certify adhesives to the D3 humidity-resistance class under EN 204:2016 require the colloidal binder to provide both dry handling strength and resistance to short-term cold-water exposure in indoor joinery and kitchen furniture subcomponents. Formulation records for D3-grade vinyl acetate-ethylene adhesives place the dispersion at 75–90 wt% of the liquid formulation, combined with 5–12 wt% of a 12–15% polyvinyl alcohol solution, 1–3 wt% of a non-phthalate plasticizer such as triacetin or dipropylene glycol dibenzoate, 0.1–0.3 wt% biocide, and 0–8 wt% calcium carbonate filler with a mean particle diameter below 10 µm. The dispersion is charged into the mixer after the separately hydrated PVOH solution has been cooled below 40°C; adding the dispersion first or at temperatures above 55°C destabilizes the protective colloid layer and can raise sieve residue above 200 µm on a 40-mesh screen. Mixing is carried out in a planetary dissolver of 500–2000 L working volume equipped with vacuum deaeration at -0.08 MPa for 20–30 min; a low-shear progressive cavity pump transfers the finished product to high-density polyethylene drums. Batch viscosity after compounding is typically adjusted with water to 7000–12000 mPa·s at 25°C; high-shear viscosity at 1000 s⁻¹ may fall below 800 mPa·s as measured by cone-and-plate rheometry, which determines transfer behaviour on roller applicators. Application of the ready-formulated adhesive onto beech strips for EN 205:2016 test assembly uses a finger-roll or roll coater at 150–220 g/m² wet weight; open times at 23°C and 50% relative humidity normally fall between 4 and 8 min depending on the PVOH content. Pressing at 0.7–1.0 N/mm² for 15–30 min at ambient temperature produces glue lines that, after 7 days conditioning at 23°C/50% RH, exceed the minimum D3 thresholds for dry and water-treated shear strength; wet loading after 4 days in cold water according to EN 205 induces cohesion failure within the dispersion film rather than adhesion loss at the wood interface, which is a required failure mode for D3 acceptance. Terminal articles include interior furniture joints, door frame subassemblies, stairs, and shopfitting panels. Filler loading above 10 wt% reduces the wet shear plateau after 4-day water storage and can produce mixed-mode failure; therefore, 8 wt% is treated as the practical upper boundary unless the wetting agent package is rebalanced. Under REACH Regulation 1907/2006/EC, the safety data sheet for the base dispersion does not list formaldehyde as an intentionally added substance and does not classify the product as an APEO-containing formulation under the manufacturer’s regulatory declaration. High-pH amine-based additives above 0.5 wt% are avoided because a pH rise above 6.5 can thicken the batch and shorten shelf life.
In flexible packaging converting lines that laminate printed paper to polyester or polyethylene film, the waterborne adhesive must dry below the film distortion threshold while retaining heat-seal-like activation at the nip. The use of VINNAPAS 5043 N as a lamination coating is based on its low film-forming temperature around 0°C, which allows coherent film formation without external coalescer additions at drying-air temperatures of 60–90°C. Typical coating formulations dilute the dispersion to a viscosity of 150–250 mPa·s at 25°C and apply it through a 60–100 LPI rotogravure cylinder or reverse-roll coater at 2–6 g/m² dry coat weight; the dispersion content of the coating liquid is 45–70 wt%, with the balance deionized water plus 0.2–0.5 wt% of a silicone-free defoamer where foam disrupts gravure cell transfer. The drying tunnel is normally segmented into three zones at 60°C, 80°C, and 90°C with air velocity 5–10 m/s; line speeds between 50 and 120 m/min are bounded by the time required for residual moisture to fall below 0.5% before the nip. The adhesive layer is reactivated by heat and pressure in the lamination nip at 70–100°C and 0.3–0.5 MPa. For food packaging, indirect-contact adhesives must comply with FDA 21 CFR 175.105 and, in the EU, Regulation (EU) No 10/2011 on plastic materials and articles intended to come into contact with food; the base dispersion’s compliance documentation should be verified for migration, and the finished laminate is tested for overall migration of ≤10 mg/dm² and specific migration limits applicable to additives. Terminal converted articles include dry-food pouches, paper-backed metallized film, and composite paper/polyethylene sachets. Defoamer addition above 0.5 wt% causes pinholes in the dried film and is not recommended. One operational boundary observed on multi-layer lamination machines is that accumulated wet adhesive on the reverse-roll doctor blade can undergo skin formation after 15–20 min idle time; when the line stops, the coating pan needs a continuous slow circulation loop to maintain a film-forming skin below 0.5 mm thickness.
Where spiral paper core winders and convolute tube machines operate at high surface speed, the dispersion is applied directly to one or more paper plies before they pass over a heated mandrel. The working liquid is prepared by diluting VINNAPAS 5043 N to 100–200 mPa·s at 25°C; the dispersion content in the applied adhesive is maintained at 60–85 wt%, with small additions of urea or glycerin at 0.5–1.5 wt% to extend open time under high air-flow and to reduce crusting on transfer rolls. Application equipment consists of a grooved steel roll running in a doctor-blade-controlled pan, with a transfer gap of 0.15–0.30 mm; coat weights range from 8 to 15 g/m² dry per ply. The core winding line operates at 40–120 m/min, with web tension set between 0.5 and 1.5 N/mm width; the adhesive must develop sufficient wet tack within 0.8–1.5 s to prevent ply separation before the mandrel cools below 50°C. Because the product is a PVOH-stabilized dispersion, high-shear application on fast winders can transiently reduce viscosity below 80 mPa·s; if the adhesive is diluted too far, strike-through to the outer ply creates blocking on the finished core. Dilution below 80 mPa·s is therefore not specified for spiral winders running above 100 m/min. Finished paper cores are tested under ISO 11093-9 for resistance to flattening; customer specifications typically require collapse resistance values above 1000 N for a 76 mm diameter core with 10 mm wall thickness, though the acceptance level is grade-dependent and is verified on the user’s own finished core specification. Terminal articles are paper cores for flexible packaging reels, film reels, textile winding cones, and industrial paper rolls.
Membrane press lamination of medium-density fibreboard profiles with PVC, polyester, or resin-treated paper foils imposes a dual requirement: the adhesive film must remain reactivatable during the membrane heating cycle and must produce a surface soundness after curing that satisfies EN 311:2005. When PVAc homopolymer adhesives are replaced by VINNAPAS 5043 N, the reduction in glass transition temperature from the PVAc range of 28–35°C to approximately 0°C shifts the minimum activation temperature downward and supports adhesion to low-energy PVC surfaces without requiring chlorinated primers. In this segment, the liquid adhesive is formulated with the dispersion at 50–80 wt%; lower levels are used when the system is a co-binder with a higher-Tg PVAc, while higher levels are selected for single-polymer furniture adhesives with higher water resistance. Additional raw materials include 5–15 wt% calcium carbonate with a top-cut particle size below 15 µm, 0.5–2 wt% of a sulfosuccinate wetting agent, and rheology modifiers to hold a viscosity of 2000–4000 mPa·s under a #4 Brookfield spindle at 20 rpm. The production line applies 60–120 g/m² wet adhesive to the MDF edge or face by roller coater or air-assisted spray; the coated parts are dried at 40–60°C for 2–5 min to a clear, non-blocking film below 1.5% residual water. Membrane press conditions are set at 80–100°C membrane temperature, 0.3–0.6 MPa pressure, and 60–180 s dwell; the hot membrane pushes the PVC foil into the adhesive while heated air activates the dispersion film. After 48 h post-curing at 23°C, the laminated surface is tested under EN 311:2005 for surface soundness; coated MDF panels intended for furniture sale must demonstrate minimum surface strength values defined in the end-use panel standard, often ≥0.9 N/mm² for boards used in high-humidity interior environments, though purchased panels must meet their individual declaration. Membrane temperatures above 110°C should be avoided because PVC foil marking and adhesive squeeze-out from the glue line become more probable. Formaldehyde emission compliance derives primarily from the substrate; the adhesive introduces no intentionally added formaldehyde, which supports E1 panel assemblies under EN 13986 and EN ISO 12460-5. Terminal articles include thermoformed cabinet doors, curved office furniture fronts, drawer fascias, and PVC-wrapped profiles.
On book casing-in lines and paper converting machines where metered rod application delivers the waterborne adhesive from a heated glue pot to the cloth or paper spine in a very short dwell, tight viscosity control is binding. The dispersion can be used as the primary binder in casing-in adhesives at 70–90 wt% of the formula, plasticized with 1–2 wt% dibenzoate or citrate plasticizer and thickened with 0.2–0.8 wt% associative polyurethane thickener to a target viscosity of 600–1200 mPa·s at 60°C as measured by a Brookfield rotational viscometer under ISO 2555. Application through a metering rod of 0.15–0.35 mm wire diameter delivers 30–60 g/m² wet adhesive to the hinge area, and the case is set immediately at 0.2–0.4 MPa in a casing-in station. Because the product has PVOH stabilizer, the glue pot temperature must be kept below 65°C to avoid brown skin formation on the pot walls; if the pot is held without agitation for more than 30 min, the surface film should be removed before restart. Thickener addition above 0.8 wt% produces stringing at the metering rod and uneven adhesive transfer to the hinge cloth. The binding line is normally run at 30–60 cases/min. Published comparative shear-resistance data for case-bound book hinge polymers under accelerated ageing is limited; specification trials are therefore run on the actual casing-in line. Compliance for the converted article is primarily mechanical and archival rather than food-contact; finished books are tested for flexible joint durability according to internal library binding standards, and raw materials are screened under REACH 1907/2006/EC and RoHS Directive 2011/65/EU where the hardcover contains electronic tags. Terminal articles include hardcover books, case-bound business stationery, and reinforced folders.
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VINNAPAS® 5043 N is an aqueous polymer dispersion based on a vinyl acetate-ethylene (VAE) copolymer, supplied by Wacker Chemie AG as a primary binder for adhesives and sealants in the flooring, construction, and lamination sectors. The dispersion is plasticizer-free, contains no added low-molecular-weight phthalate plasticizers, and is stabilized without added alkylphenol ethoxylates. It forms a film at ambient temperature through ethylene-based internal plasticization rather than through external coalescing-solvent demand. The product is designed for compounds requiring high filler acceptance, low transfer viscosity, and adhesion to plasticized PVC, bituminous substrates, and non-porous surfaces. Manufacturer control values and the corresponding test methods are given in Table 1.
| Property | Test method | Control range / typical value |
|---|---|---|
| Solids content | ISO 3251 (2 h, 105 °C) | 52–54% |
| pH at 25 °C | ISO 976 | 4.0–6.0 |
| Viscosity, Brookfield RVT, spindle 3, 20 rpm, 25 °C | ISO 2555 | 1000–3000 mPa·s |
| Minimum film-forming temperature | DIN ISO 2115 | approximately 0 °C |
| Density at 25 °C | ISO 2811 | approximately 1.06 g/cm³ |
These control ranges should be read together with the certificate of analysis for each production lot because VAE dispersion viscosity is not solely a molecular-weight marker. Viscosity shifts with pH, particle-size distribution, surfactant equilibrium, storage history, and degree of aeration. A batch near the lower pH limit may exhibit longer shelf stability but lower tolerance to cationic contamination, while a batch near the upper solids limit may require higher dispersion force during thickener letdown. The certifying laboratory data therefore determine the adjustment of thickener demand, defoamer dosage, and transfer-pump selection.
The principal difference from plasticized poly(vinyl acetate) homopolymer dispersions is the absence of external plasticizer in the binder. Homopolymer PVAc dispersions commonly require dibutyl phthalate, diisononyl phthalate, or similar coalescing plasticizers to achieve film formation below 10 °C. These low-molecular-weight additives migrate over time, can attack plasticized PVC floor coverings, and reduce long-term heat resistance. VINNAPAS® 5043 N uses ethylene comonomer to depress the minimum film-forming temperature to approximately 0 °C, so film formation and low-temperature flexibility are obtained without plasticizer bleed. Compared with higher-viscosity VAE dispersions, the 1000–3000 mPa·s viscosity range supports high filler loading and easier transfer by low-shear diaphragm or progressive-cavity pumps.
Film formation in VAE dispersions is controlled by polymer-particle deformation above the effective glass transition. In vinyl acetate homopolymers, particle coalescence is limited at typical construction temperatures unless a coalescing solvent or external plasticizer is added. Ethylene segments in VINNAPAS® 5043 N create internal free volume and lower the minimum film-forming temperature. Under DIN ISO 2115, the product forms a film at approximately 0 °C; at 5 °C and above, film consolidation proceeds without external coalescent. Below 0 °C, polymer-particle mobility becomes insufficient and the dried film develops cracks and reduced cohesive strength. This establishes the operational boundary for cold-weather flooring adhesives: site storage must not freeze, and application below 5 °C requires heated substrate, a heated transport line, or an insulated mixing vessel.
Ethylene distribution also affects compatibility with tackifier dispersions. Rosin-derivative and hydrocarbon tackifier dispersions used to increase wet tack should be pre-diluted to 40–50% solids before addition to the binder. Direct addition of high-solids tackifier can generate transient ionic shock at the dispersion interface, producing visible gel specks larger than 100 µm. In production, inline cartridge filtration at 100–250 µm is standard before spray heads, roller-coater gaps, or filling lines. Coagulum retained on the filter is an early indication of pH drift, defoamer incompatibility, or microbial degradation.
Adhesion to plasticized PVC sheet is evaluated after a seven-day cure at 23 °C and 50% RH using a 90° peel test according to ASTM D6862. In wet-set flooring adhesive formulations, the binder is typically loaded at 100 parts by weight, extended with 80–120 parts of fine ground calcium carbonate, and thickened with a polyacrylic acid or cellulose ether. Failure mode is more informative than peak peel force: cohesive failure within the adhesive film indicates adequate substrate wetting, while interfacial adhesive failure at the PVC surface may indicate insufficient open time, plasticizer contamination, or an over-dried film. Published data for this specific configuration is limited; plant trials should include peel series on actual flooring lots and after accelerated aging at 40 °C for 7 days.
On bituminous substrates, ethylene flexibility provides conformability without external plasticizer and improves wetting on low-energy surfaces relative to PVAc homopolymer dispersions. However, bituminous surfaces may carry cationic residues, oils, or humectants that destabilize an anionically stabilized dispersion. Adhesion tests on substrate coupons are required before specifying the product for cutback-adhesive overlays, asphalt repair membranes, or flooring over fresh asphaltic concrete. Because the binder contains no added dibutyl phthalate or diisononyl phthalate, the risk of staining of vinyl floor coverings after long contact times is reduced compared with plasticized PVAc adhesives.
Solvent-borne contact adhesives are replaced by VINNAPAS® 5043 N in spray lamination, panel bonding, and foam-to-board assemblies where VOC reduction is required. The aqueous system requires a longer flash-off interval than solvent controls. At a wet-film weight of 120–200 g/m², the dry-to-tacky interval is typically 10–30 minutes at 23 °C and 50% RH, whereas a typical solvent-borne control develops tack within a few minutes. The film changes from white to translucent; bonding should occur while the surface retains finger tack. Over-drying beyond 60 minutes produces a non-tacky surface and low green strength. Production lines must therefore adjust open-time scheduling or add a retarding humectant such as propylene glycol when ambient humidity falls below 40% RH.
Air-assisted airless spray equipment with nozzle tips of 0.28–0.48 mm and fluid pressure of 50–80 bar is used for large-area application. Electrostatic spray is not recommended because the aqueous dispersion has sufficient conductivity to complicate charge retention. Loop tack on stainless steel according to ASTM D6195 is lower during the first 30 minutes after bonding than solvent-borne controls, but increases as water leaves the film. Equipment cleanup uses water before the film crosslinks; dried film requires mechanical cleaning or a solvent-based cleaner suitable for VAE polymer. Because initial tack develops more slowly, nip pressure and press dwell time on panel lamination lines must be increased relative to solvent-borne process settings.
VINNAPAS® 5043 N exhibits pseudoplastic flow; low-shear Brookfield viscosity does not predict behavior under knife-over-roll, roller coating, or trowel application. Open time is extended more effectively by raising formulation pH to 8.0–8.5 with an alkali-swellable acrylic thickener than by increasing total solids. The pH shift increases serum viscosity, slows water loss, and improves the wet edge. However, pH above 9.0 can hydrolyze vinyl acetate ester groups, increasing acetate ion content and eventually reducing adhesive heat resistance. Formulators should monitor pH after thickener addition and after 24 hours of aging because thickener hydration continues after initial mixing.
Cellulose ethers increase water retention on porous concrete but reduce wet tack faster than alkali-swellable thickeners because free water is immobilized. In plant-scale mixing with a planetary mixer and wall scraper, fillers and thickener are pre-dispersed in water, and the polymer dispersion is added last to limit mechanical stress. High-speed dissolver stages should be limited in duration because excessive shear can permanently reduce particle-size integrity and lower viscosity. Vacuum deaeration at 150–300 mbar for 10–20 minutes removes entrained air; without deaeration, microfoam causes surface defects in roller coating and reduces density-based yield measurements.
Foaming is controlled with mineral-oil or silicone defoamers at 0.1–0.3 wt%. Silicone defoamers improve leveling but can create fisheye defects on non-porous PVC; mineral-oil defoamers are less likely to produce surface defects but may require higher dosage. Defoamer should be added to the water phase before the polymer dispersion because shock addition to the neat dispersion can create localized hydrophobic spots that appear as microgels. Filler tolerance is adequate for calcium carbonate levels up to 80–120 phr; above 150 phr, wet tack and peel strength decrease sharply because the binder volume fraction falls below the percolation threshold for film continuity.
The product is not intended for continuous water immersion or exterior ponding without additional crosslinking or water-resistant tackifier. Dried films may water-whiten because hydrophilic surfactant and acetate groups rehydrate; immersion in water for 24 hours can reduce peel strength by more than 30% unless a water-resistant additive is incorporated. For moisture-cure flooring adhesives, VINNAPAS® 5043 N is not a reactive isocyanate component; compatibility with polymeric MDI or silane-terminated prepolymers is limited by residual water and anionic surfactant content. Formulators evaluating hybrid systems should run a sealed-vessel viscosity build test or CO₂ evolution test before scaling.
Storage is recommended at 5–35 °C in sealed containers. Freezing destroys the dispersion through ice-crystal destabilization; storage above 40 °C accelerates skinning and sediment formation. The product should be transferred with low-shear diaphragm or progressive-cavity pumps rather than high-speed centrifugal pumps. In-line filters of 100–250 µm are standard before spray or roller-coat application. The product should not be combined with cationic surfactants, polyvalent metal salts, or high-acid additives that reduce pH below 3.0, because these conditions can produce gel specks. Manufacturers formulating for indirect food-contact adhesives may evaluate finished formulations under FDA 21 CFR 175.105; raw-dispersion compliance alone does not confer final-article suitability.