| HS Code | 188207 |
| Product | GW-706 High-Viscosity VAE Emulsion |
| Chemical Family | Vinyl Acetate-Ethylene Copolymer |
| Appearance | White milky liquid |
| Solid Content | 50 ± 1% |
| Viscosity Brookfield 25 C | 15000 ± 5000 mPa·s |
| Ph | 5.0 - 7.0 |
| Glass Transition Temperature Tg | -5°C |
| Minimum Film Forming Temperature | 0°C |
| Particle Size | 0.5 - 1.5 μm |
| Residual Monomer Content | ≤ 0.1% |
As an accredited GW-706 High-Viscosity VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in 200 kg drums with sealed lids, labeled for safe handling and storage of GW-706 High-Viscosity VAE Emulsion. |
| Container Loading (20′ FCL) | 20′ FCL loaded with IBCs/drums of GW-706 VAE emulsion, secured and braced for safe transport. |
| Shipping | GW-706 High-Viscosity VAE Emulsion ships in sealed drums or IBC totes to prevent leakage. Protect from freezing and excessive heat during transit. Standard ground freight is suitable; keep containers upright and dry. Ensure proper labeling for industrial use. |
| Storage | Store GW-706 High-Viscosity VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area. Avoid direct sunlight, heat sources, and freezing temperatures; ideal storage is between 5–35°C. Keep away from strong oxidizers. Stir gently before use if separation occurs. Use within six months of receipt for optimal performance. |
| Shelf Life | Shelf life is typically 12 months from manufacture if stored sealed, cool, and frost-free. |
A cementitious slurry modified with a high-viscosity vinyl acetate-ethylene copolymer achieves functional waterproofing integrity when the polymer-to-cement ratio is maintained within a narrow rheological window. In two-component systems utilizing GW-706, a dispersion exhibiting a Brookfield viscosity of 62,000–78,000 mPa·s (#6 spindle, 20 rpm, 25°C) and a minimum film-forming temperature of ~0°C, the liquid component is typically formulated with 0.8–1.2 parts by weight of the emulsion per 1.0 part of the powdered cementitious binder. Deviation below 0.8 parts results in a discontinuous polymer network and elongation at break measured per ASTM D6083 dropping beneath 60%, while exceeding 1.2 parts introduces prolonged surface tack, retarded cement hydration, and a capillary water absorption coefficient above 0.1 kg/(m²·h⁰·⁵) when tested under EN 1062-3. Compliance is established through ASTM D6083 Type II, EN 1504-2 surface protection systems, and GB/T 23445 Type II, which mandate tensile adhesion strength via ASTM C1583 exceeding 1.0 MPa on saturated concrete and crack-bridging ability at −10°C over a dynamic opening of ≥0.5 mm. The downstream manufacturing process for the liquid component proceeds in a planetary mixer equipped with a paddle-and-scraper tool rotating at 250–350 rpm, where GW-706 is blended with a polymethylsiloxane defoamer dosed at 0.3–0.5 wt%, a coalescent such as texanol at 4–6% of solids, and a polycarboxylate superplasticizer to extend open time. Once the dispersion is stable, it is packaged separately from the dry blend of type 42.5R ordinary Portland cement, 80–120 mesh quartz sand, and a cellulose ether rheology modifier. At the job site, the two components are combined in a low-shear mixer operating at 300–500 rpm for 3–4 minutes; high-speed dispersion beyond 800 rpm induces irreversible shear degradation of the latex particles, evidenced by a viscosity collapse of more than 30% and the formation of microfoam that cannot be fully broken by vacuum deaeration. The pot life at 23°C is typically 90–120 minutes, after which the exothermal hydration peaks near 55°C and must be kept below 60°C through the use of a retarder to prevent thermal destabilization of the polymer film during the critical coalescence phase. Finished articles include flexible cementitious waterproofing membranes applied by trowel or spray onto green roofs, basement retaining walls, and potable water tanks following an additional NSF/ANSI 61 certification assessment.
The failure mode in high-performance tile adhesives exposed to cyclic freeze-thaw loads often originates not from the cement matrix but from the relaxation capacity of the incorporated polymer. When GW-706 is incorporated into a two-component C2S1-classified adhesive conforming to ISO 13007-1 and tested per EN 12004, the recommended addition ratio of the high-viscosity emulsion is 0.25–0.30 parts by weight per 1.0 part of the dry powder blend, translating to a polymer solids content of 5–7% relative to total dry mass. At this level, the transverse deformation under EN 12002 can exceed 2.5 mm, and the tensile adhesion strength after water immersion (EN 1348) stabilizes above 1.0 MPa. The technical boundary emerges in thermal shock cycling between −15°C and +70°C, where the glass transition temperature of the VAE copolymer, positioned near 0°C, triggers a modulus jump that, if not compensated by the choice of a more flexible cement modification, reduces shear adhesion to porcelain tiles to less than 0.5 MPa after 50 cycles per EN 1348 with freeze-thaw conditioning. Production-scale batching on a forced-action mixer with a vertical shaft and a planetary gear drive—such as a 60-liter Hobart-type unit at 140–185 rpm—requires the liquid admixture to be poured into the bowl before the powder to prevent clumping, followed by 180 seconds of wetting, a 3–5 minute maturation pause, and a final 30-second re-mix. GW-706’s pseudoplastic profile yields a low-shear viscosity during manual trowel application that limits slip to ≤0.5 mm on wall tiles when measured according to EN 1308, yet the viscosity recovers sufficiently within 10 seconds of rest to hold notched ridges without slump. An incompatibility exists with high-alumina cement contents beyond 10% of the binder blend, where the rapid aluminum hydroxide formation can extract protective colloid and cause instantaneous coagulation; this has been documented on production lines as a sudden increase in mixing torque exceeding 40 N·m in a 100-liter horizontal mortar mixer. Terminal products span thin-bed tile adhesives for large-format porcelain slabs in exterior ventilated facades under ETAG 004 guidelines and rapid-setting levelling compounds for heated screeds.
An exterior elastomeric coating formulated with GW-706 achieves crack-bridging beyond 1200 µm at −10°C only when the polyvinyl alcohol-stabilized dispersion is dosed at 25–35 wt% of the total wet formulation and the pigment volume concentration is constrained within 25–35%, avoiding the region above 40% PVC where a discontinuous binder phase causes elongation per ASTM D2370 to plummet from 300% to below 50%. Compliance is verified against ASTM D6900 for exterior elastomeric wall coatings and ISO 4618-1 for terminology plus associated test methods such as ISO 7783 for water-vapor diffusion, where the coating must demonstrate an equivalent air-layer thickness Sd ≥50 m for carbonation protection. The manufacturing process is executed in a variable-speed high-speed disperser with a tooth-blade impeller rotating initially at 600–800 rpm for liquid pre-mixing, then raised to 1500–2000 rpm for 20–30 minutes to achieve a Hegman grind of 4–5 on the pigment paste composed of titanium dioxide and coarse calcium carbonate extender. Temperature must be monitored and kept under 45°C during dispersion because GW-706’s colloidal stability degrades if the jacket temperature exceeds 50°C, manifesting as a 10–15% loss in Brookfield viscosity and the appearance of grit on a 50 µm filter. After a cooling phase, the letdown incorporates an additional coalescent charge of 5–8% on emulsion solids and a urethane thickener to rebuild low-shear viscosity to 110–120 Krebs Units; failure to incorporate the thickener at a shear rate below 200 s⁻¹ can create a viscosity stratification defect observed as sag resistance deterioration in vertical wall trials. Finished products are high-build elastomeric topcoats for precast concrete panels subjected to dynamic wind loads and coastal salt spray, where adhesion measured per ASTM D4541 must remain above 1.2 MPa after 2000 hours of QUV-B exposure.
Multi-layer paperboard packaging adhesives that replace hot-melt with an aqueous cold-applied system benefit from the instantaneous tack of GW-706 without the safety and thermal-cost burdens of a heated tank. The neat emulsion, after dilution to a Ford cup 4 viscosity of 45–60 seconds at 25°C, is deposited via a three-roll transfer coater or an air-knife coater at a dry coatweight of 18–25 g/m² per side. Regulatory conformance is established through U.S. FDA 21 CFR 176.170 for components of paper and paperboard in contact with aqueous and fatty food, supplemented by EU Framework Regulation (EC) No. 1935/2004 and BfR Recommendation XIV for polymer dispersions. The converting line operates at 80–150 m/min with a drying tunnel profile that ramps from 90°C to a peak of 130°C over 40–60 seconds; insufficient drying manifests as blocking in the rewind roll when the residual moisture exceeds 2.0%. Terminal articles include pharmaceutical folding cartons for blister packs and frozen-food sleeves where the high initial shear strength—above 500 N/m in a peel test based on TAPPI T 494—prevents ply separation during rapid filling operations.
For a secondary backing applied to tufted cut-pile carpet, GW-706 is mechanically frothed to a foam density of 350–700 g/L using a continuous Oakes mixer rotating at 400–800 rpm rotor speed with a counter-pressure of 1.5–3.0 bar, where the emulsion constitutes 80–85% dry weight of the binder compound, with a calcium carbonate filler loading of 200–350 phr. The foam must exhibit a half-life of ≥15 minutes prior to coating to prevent pre-mature collapse on the knife-over-roll coater, and GW-706’s high viscosity at low shear provides the film elasticity needed to hold the foam cell structure during the initial drying stage at 170–180°C for 3–5 minutes in a stenter frame. Performance qualification includes ISO 10310 for tuft withdrawal force exceeding 25 N and ASTM D1335 for tuft bind, along with a slip resistance coefficient above 0.4 per ASTM D2047. This application enters its shallow specification zone when the carpet construction is a low-pile needled felt, where simple pad-dry application at 30% binder pickup replaces the frothing complexity. Finished goods encompass commercial modular carpet tiles with bitumen-compatible secondary backings and automotive interior mats meeting FMVSS 302 flammability class.
Rotary-screen printing pastes thickened exclusively with a synthetic alkali-swellable thickener often exhibit sharp-edged definition loss due to inadequate viscosity recovery after the squeegee shear; the addition of 5–15 wt% GW-706 to the paste restores a thixotropic hysteresis loop area above 1500 Pa·s⁻¹ when measured on a cone-and-plate rheometer from 0.1 to 100 s⁻¹ and back, maintaining line width variation below 12% on a 100-count cotton fabric. The paste is prepared in a planetary dissolver where the emulsion is post-added to the pre-gelled thickener at ambient temperature under a peripheral speed of 4–8 m/s, and the final pH is adjusted with ammonia to 4.2–4.8 to secure colloidal stability of the acetate-containing copolymer; deviation to pH 3.5 causes a 25% irreversible drop in plastic viscosity. Conformity to human-ecological safety demands is addressed via OEKO-TEX Standard 100 annex 6 for product class I infant articles, and the absence of formaldehyde donors is verified through EN ISO 14184-1. After printing at 20–40 m/min, the fabric passes through a multi-zone dryer with an air temperature profile of 130–150°C for 90–180 seconds to achieve film coalescence and crosslinking with an optional polyfunctional aziridine fixer at 0.5–1.0% on binder solids. End products are wash-resistant pigment prints for upholstery and fashion apparel that withstand 40 cycles of domestic laundering at 60°C per ISO 6330 without significant crocking, tested per AATCC 8.
| GW-706 / Cement (w/w) | Tensile Strength (MPa) ASTM D412 | Elongation (%) ASTM D412 | Water Impermeability EN 12808-4 (0.3 MPa, 30 min) |
|---|---|---|---|
| 0.6:1 | 2.8 | 52 | Fail: leakage after 12 minutes |
| 0.8:1 | 2.1 | 118 | Pass |
| 1.0:1 | 1.6 | 245 | Pass |
| 1.2:1 | 1.2 | 320 | Pass, surface tack at 48h |
| Application | Standard / Regulation | Key Metric | Requirement |
|---|---|---|---|
| Polymer-Cement Waterproofing | ASTM D6083 Type II | Elongation at -26°C | ≥ 20% |
| Thin-Set Tile Adhesive | ISO 13007-1 C2S1 | Adhesion after water immersion | ≥ 1.0 MPa |
| Elastomeric Wall Coating | ASTM D6900 | Elongation at -10°C | ≥ 100% |
| Paperboard Lamination | FDA 21 CFR 176.170 | Global migration limit | ≤ 10 mg/dm² |
| Carpet Backing | ISO 10310 | Tuft withdrawal force | ≥ 25 N |
| Textile Print Paste | OEKO-TEX 100 Class I | Formaldehyde content | Not detectable per EN ISO 14184-1 |
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GW‑706 High‑Viscosity VAE Emulsion is an internally plasticized, surfactant‑stabilized vinyl acetate–ethylene (VAE) copolymer dispersion supplied at 63 ± 1 % solids (ISO 3251) with a Brookfield RVT viscosity of 12 000–18 000 mPa·s at 25 °C (spindle 6, 20 rpm, ASTM D2196). The emulsion is free of external plasticizers and alkylphenol ethoxylates; film formation occurs via ethylene‑induced internal plasticization at a minimum film‑forming temperature of 0 °C (MFFT, ISO 2115) and a glass transition temperature of approximately −5 °C (DSC, ISO 11357‑2). The pH resides between 4.5 and 5.5 (ISO 976), and the average particle diameter spans 0.5–0.8 µm (laser diffraction, ISO 13320). Designed as a high‑tack, high‑rheology binder, GW‑706 is deployed in D3/D4 wood flooring adhesives, polymer‑modified cementitious waterproofing slurries, and single‑coat parquet adhesives where sag resistance and filler‑holding capacity are mandatory. In these domains, the product differs from low‑viscosity VAE grades such as GW‑406 (solids 55 %, viscosity 1500–3000 mPa·s) by enabling filler loading up to 400 phr of calcium carbonate without sedimentation and by delivering wet film thicknesses exceeding 800 µm in a single trowel pass without slump. Compared with typical styrene‑acrylic emulsions, GW‑706 provides superior adhesion to unprepared beech and oak substrates without chlorinated‑solvent primers, a consequence of the high vinyl acetate content that forms multiple hydrogen bonds with cellulose hydroxyl groups. The emulsion carries no hazard classification under CLP Regulation (EC) No 1272/2008 and complies with the low‑VOC criteria of the German AgBB scheme (< 0.3 % residual monomer).
The defining rheological feature of GW‑706 is its pronounced pseudoplasticity: the low‑shear viscosity of 12 000–18 000 mPa·s drops to 3 000–5 000 mPa·s under the shear rates generated by a notched trowel (10–50 s⁻¹), as measured on a controlled‑stress rheometer (cone‑plate, 40 mm, 1 °). This shear‑thinning behaviour allows a high static yield stress that arrests filler settling, yet permits easy spreading without the addition of associative thickeners. Acrylic emulsions of equivalent solids (63 %) typically exhibit near‑Newtonian flow and require post‑thickening with polyurethane‑based HEUR rheology modifiers, which can compromise wet adhesion and retard film formation in high‑humidity conditions (RH > 80 %). Styrene‑butadiene latexes can achieve similar shear‑thinning but often require higher coalescent dosages and contribute to higher VOC profiles. GW‑706 also supports exceptionally high filler loads: trials on a planetary dissolver (Netzsch MasterMix, 7.5 kW) have demonstrated that 400 phr of fine calcite (D₅₀ 2 µm) can be incorporated without exceeding a Hegman grind of 4 NS, whereas analogous low‑viscosity VAE emulsions exhibit phase separation at 250 phr. The following table summarizes the compositional and rheological contrast.
| Property | GW‑706 (High‑Viscosity VAE) | GW‑406 (Standard VAE) | SA‑202 (Styrene‑Acrylic) |
|---|---|---|---|
| Solids (ISO 3251) | 63 ± 1 % | 55 ± 1 % | 50 ± 1 % |
| Brookfield viscosity (ASTM D2196, 25 °C, sp. 6/20 rpm) | 12 000–18 000 mPa·s | 1500–3000 mPa·s | 200–600 mPa·s |
| MFFT (ISO 2115) | 0 °C | 0 °C | 18 °C |
| Tg (DSC, ISO 11357‑2) | −5 °C | +5 °C | +25 °C |
| Particle size D₅₀ (ISO 13320) | 0.6 µm | 0.8 µm | 0.15 µm |
| Maximum calcite loading before sedimentation (static, 7 days) | 400 phr | 250 phr | 300 phr |
| Freeze–thaw stability (closed container, −5 °C/23 °C, 5 cycles) | add 5 % ethylene glycol | add 5 % ethylene glycol | inherently stable |
The absence of external coalescents in GW‑706 reduces the occupational exposure risk during application in confined spaces; total VOC content remains below 0.5 % (ISO 11890‑2). Because the ethylene comonomer provides permanent flexibility, the film does not embrittle over time due to plasticizer migration, a documented failure mode in PVAc homopolymer adhesives after 5‑year indoor ageing at 40 °C (EN 14292).
When formulated as a filled wood adhesive, GW‑706 meets the requirements of durability classes D3 and D4 of EN 204/205 with the addition of an acidic metal salt catalyst. In a typical production‑scale twin‑planetary mixer (Ross PDM‑2, 20 L), a reference formulation comprising 100 pbw emulsion, 200 pbw calcite filler, 0.5 pbw defoamer (polyether siloxane), and 3 pbw aluminium chloride solution (50 % in water) yields a stable paste with a pot life exceeding 4 hours at 23 °C. The high initial viscosity prevents sag on vertical oak blocks, permitting one‑step installation without temporary pinning. After 7 days’ conditioning at 23 °C/50 % RH followed by 4 days’ immersion in cold water (20 ± 2 °C), the tensile shear strength measured on beech to EN 14256 reaches 2.8 MPa with cohesive failure in the wood substrate. In contrast, the same formulation prepared with a low‑viscosity VAE (GW‑406) fails to exceed 1.2 MPa under identical preparation conditions due to filler sedimentation and internal de‑wetting at the tile–adhesive interface.
The creep resistance under sustained load (EN 14257, 7.2 kg dead load, 23 °C, 7 days) remains below the 0.5 mm limit when the aluminium chloride catalyst is used; without catalyst, creep exceeds 2.0 mm and the formulation is acceptable only for D1/D2 service. It is critical to avoid accidental contamination with amines or ammonia vapour during storage and compounding, because amine‑catalysed transesterification of the vinyl acetate units leads to premature cross‑linking and spot‑gelation within the closed container—a phenomenon observed on a 500 kg IBC stirred batch when a residual monoethanolamine cleaning agent remained in the filling line.
GW‑706 can be integrated into Portland cement‑based mortars to produce flexible crack‑bridging slurries and repair systems. The high‑viscosity character reduces mixing‑water demand in a two‑component blend; at a polymer‑cement ratio (p/c) of 0.15, the water‑demand reduction compared with a standard VAE (GW‑406) is 12 %, allowing a lower water/cement ratio and compensating for the strength‑retarding effect of the latex. A mortar prepared with CEM I 42.5 R (EN 197‑1), silica sand (0.1–0.5 mm), emulsion, and a tributyl phosphate defoamer (0.3 % on emulsion) exhibits the following properties as a function of dosage. The data were obtained on a Collomix XM‑2 forced‑action mixer with 30 L batch size under laboratory conditions.
| p/c ratio | Flow table spread (EN 1015‑3) | Vicat initial set (EN 196‑3, mm) | Compressive strength 28 d (EN 12190) | Flexural strength 28 d (EN 196‑1) |
|---|---|---|---|---|
| 0 (control) | 145 ± 5 mm | 195 min | 48.0 N/mm² | 7.2 N/mm² |
| 0.10 | 165 ± 5 mm | 210 min | 41.5 N/mm² | 8.8 N/mm² |
| 0.15 | 175 ± 5 mm | 240 min | 36.0 N/mm² | 9.5 N/mm² |
| 0.20 | 190 ± 5 mm | 290 min | 29.2 N/mm² | 10.2 N/mm² |
The emulsion tolerates the high‑pH environment of hydrating cement; however, the early release of calcium hydroxide can destabilise the colloidal dispersion if mixing is interrupted and the paste is left unstirred for more than 15 minutes. A continuous feed of dry mortar powder into the liquid emulsion under high‑shear disperser (rotor‑stator gap 0.5 mm) avoids flocculation. The maximum recommended p/c is 0.20; beyond this level, the initial set is retarded by more than 4 hours and shrinkage cracking may occur because the polymer film formation lags behind cement hydration. Additionally, mixing water must contain less than 2000 ppm calcium ions (as CaCO₃) to prevent instantaneous electrostatic coagulation—a limit routinely exceeded when using hard well‑water in certain Mediterranean production sites.
In high‑build, knife‑applied waterproofing membranes formulated with GW‑706 and 0.1–0.6 mm quartz sand, the crack‑bridging ability at 23 °C exceeds 0.8 mm (EN 14891, method with static crack) when the coating thickness reaches 2 mm. After 1 day’s dry curing followed by 7 days’ immersion in water, the adhesion to concrete substrate (EN 1542) remains at 1.2 N/mm², with failure occurring cohesively within the membrane. Such wet adhesion is not achievable with PVAc homopolymer emulsions, which undergo hydrolysis in alkaline cementitious environments and lose bond strength to less than 0.3 N/mm² after 48 hours’ water contact. This performance envelope, combined with film formation at 0 °C, allows the emulsion to be used in external waterproofing systems that must remain functional during spring and autumn temperature swings, provided the membrane is protected from direct UV radiation until top‑coated with a reflective layer conforming to EN 1504‑2.