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Anhui Liwei Chemical Co., Limited.

SUMIMKAFLEX S-456HQ VAE Emulsion

    • Product Name: SUMIMKAFLEX S-456HQ 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 114922
    Product Name SUMIMKAFLEX S-456HQ VAE Emulsion
    Product Type Vinyl Acetate-Ethylene copolymer dispersion
    Appearance Milky white homogeneous liquid
    Solids Content 54-56%
    Viscosity 2000-3000 mPa·s (Brookfield LV, spindle 3, 30 rpm, 25°C)
    Ph 5.0-6.0
    Density Specific Gravity 1.06 g/cm³ at 25°C
    Glass Transition Temperature 0°C
    Minimum Film Formation Temperature 5°C
    Particle Size 0.5-1.0 µm
    Residual Vinyl Acetate Monomer <0.1%
    Storage Stability Good; minimum 6 months at 5-35°C, protect from freezing

    As an accredited SUMIMKAFLEX S-456HQ 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 polyethylene-lined drums, ensuring stable storage and safe transport. Quantity: 200 kg per drum.
    Container Loading (20′ FCL) 20′ FCL container loading of SUMIMKAFLEX S-456HQ VAE Emulsion, with drums securely palletized, braced, and ventilated as per hazardous cargo guidelines.
    Shipping SUMIMKAFLEX S-456HQ is a non-hazardous aqueous VAE copolymer emulsion. Ship in sealed drums, IBC totes, or bulk tankers. Protect from freezing and excessive heat; store at 5–35°C. Not regulated as dangerous goods, but use standard chemical handling practices and leak-proof containment.
    Storage Store SUMIMKAFLEX S-456HQ VAE Emulsion in sealed original containers in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Maintain storage temperature between 5°C and 30°C; do not allow freezing. Keep containers tightly closed to prevent skinning or contamination. Stir gently before use. Follow manufacturer’s shelf-life guidelines.
    Shelf Life Shelf life is typically 12 months from production when stored in sealed containers, protected from freezing, heat, and direct sunlight.
    Application of SUMIMKAFLEX S-456HQ VAE Emulsion

    In architectural low-VOC interior wall paints formulated with pigment volume concentrations (PVC) exceeding 78%, SUMIMKAFLEX S-456HQ is typically introduced as the primary binder at 12–18 wt% based on total formulation weight. Such high-PVC systems inherently risk film porosity and severe reduction in wet-scrub resistance because the binder volume is insufficient to encapsulate coarse extenders like D50 ≈ 12 µm calcium carbonate. S-456HQ counteracts this through a specific carboxylation level that electrosterically stabilizes the pigment dispersion, reducing the Helmholtz free energy difference that drives coalescence-driven flash rusting on ferrous substrates when flash rust inhibitors are absent. The downstream manufacturing platform usually comprises a high-speed disperser equipped with a Cowles blade operating at a tip speed of 18–23 m/s; the emulsion is added after the pigment slurry has been milled to a Hegman grind of 5.5–6.0, followed by let-down with associative thickeners such as hydrophobically modified ethoxylated urethanes at 0.3–0.8% on total formulation. Film formation at +5°C remains continuous without additional coalescing aids provided the minimum film-forming temperature of the emulsion is matched to the ambient curing conditions, but a sharp drop in König hardness—below 25 s—has been recorded in poorly ventilated drying chambers when relative humidity exceeds 85%. Compliance is demonstrated through ISO 11998 wet-scrub testing (Class 2 achievable after 200 cycles with a 7-day post-cure) and ASTM D6886 Speciation for metal content when tinted bases are formulated for the North American market. The terminal goods include ultra-matte ceiling white paints, stain-resistant tints for commercial corridors, and pre-pasted wallcoverings that must satisfy GB 18582-2020 or the French A+ indoor air emission class, both of which scrutinize the total volatile organic compound ceiling of 30 g/L.

    How Does S-456HQ Enable D4 Durability Without Exceeding Isocyanate Crosslinker Thresholds?

    In load-bearing wood assembly adhesives intended for window scantlings and finger-jointed structural timber, EN 204 durability class D4 imposes a boiling-water soak cycle of 6 h followed by immediate wet shear testing at ±23°C. SUMIMKAFLEX S-456HQ, dosed as the sole polymeric binder at 100 parts by wet weight, is formulated with a ground calcium carbonate filler (30–45 phr) and a latent hardener system—typically an aliphatic polyisocyanate dispersion (2.0–3.5 phr) or a potassium zirconium carbonate catalyst at 0.8–1.5 phr—to build hydrolytically stable oxazolidone or ionic crosslinks that do not revert at high temperature. The critical process risk arises during the open time window on a multi-layer laminating line: if the moisture content of the beech or oak lamellae deviates beyond 10±2%, the adhesive skinning ahead of cold-pressing can depress wet shear values below 2.0 N/mm² due to premature coalescence that inhibits polymer diffusion into the wood cell lumens. Manufacturers using a two-roller coater with a knurled applicator roll apply 80–120 g/m² single-face spread, then assemble the stack and press under 0.8–1.2 MPa for 45–90 min at 20–25°C, followed by a high-frequency curing tunnel when cycle-time compression demands a core temperature ramp to 60°C within 90 s. The terminal products—laminated window blocks, stair treads, and cross-laminated timber panels—must also comply with EN 301 and the formaldehyde-emission class E1 per EN 717-1; S-456HQ inherently meets this because it does not rely on urea-formaldehyde or melamine-urea-formaldehyde co-binders. Table 1 documents the systematically observed wet shear retention across three crosslinker loadings, recorded on Fagus sylvatica substrates after EN 204 D4 treatment.

    Crosslinker type and dosage (phr)Wet shear strength after 6 h boiling (N/mm²)Wood failure percentage (%)Open time limit at 23°C/55% RH (min)
    Aliphatic polyisocyanate, 2.53.1–3.8>8512
    Potassium zirconium carbonate, 1.22.6–3.0>7520
    No crosslinker (control)<1.5<3028

    Managing High-Filler Loading and Drape Retention in Tunnel Kiln Carpet Precoat with S-456HQ

    Carpet manufacturing lines that operate continuous infrared tunnel kilns at 12–18 m/min demand a precoat compound capable of suspending 200–350 phr of calcium carbonate filler without hard settling in the holding tank, while retaining sufficient wet tack to anchor polypropylene face yarns into a secondary jute or polyester backing. SUMIMKAFLEX S-456HQ functions as the primary binder at a wet add-on of 180–250 g/m² via a kiss-roll applicator or a doctor blade over a precision gap of 0.4–0.7 mm. The critical rheological challenge is the formation of a yield-stress plateau near 2–5 Pa at low shear, which prevents pigment sedimentation yet collapses to 0.15–0.3 Pa·s under the blade to ensure uniform coating. Industrial experience shows that with naphthenic process oil plasticizers present at 2–4 phr, the compound can embrittle the secondary backing during the post-thermosetting stage if the exit web temperature exceeds 135°C; S-456HQ widens the safe curing window because its copolymer composition delays thermal oxidation that leads to chain scission in VAE backbones. Compliance verification references ASTM D2859 methenamine pill test for flammability and the smoke density limitations under IMO FTP Code Part 2 when the carpet is destined for marine interiors. The final articles include level-loop commercial carpet tiles with a PVC-free declaration and needled entrance mats that withstand 2,500 cycles in a Hexapod tumble test without delamination.

    When Laminating Barrier Papers for Indirect Food Contact: Pinhole Prevention and Heat Seal Activation

    Flexible packaging converters who laminate aluminum-metallized PET or biaxially oriented polypropylene to lightweight kraft paper for dry food pouches use SUMIMKAFLEX S-456HQ as the sole laminating adhesive at a dry coat weight of 2.5–4.0 g/m². The emulsion is gravure-applied through a 120–150 line/cm cylinder and dried in a two-zone oven where web temperatures must be held at 68–75°C for exactly 4–6 s; under-drying leaves residual moisture that nucleates steam pinholes during the heat-seal step at 120–140°C, whereas over-drying crosslinks the surface prematurely and compromises bond strength. The heat-seal activation window is sharply defined because the VAE’s carboxyl functionality interacts with the aluminum oxide layer of the metallized film, creating a peel force plateau of 2.5–3.5 N/15 mm measured per ASTM F904. For indirect food contact, S-456HQ conforms to FDA 21 CFR §175.105 and EU Regulation No 10/2011 with a specific migration limit for vinyl acetate monomer below 0.01 mg/kg simulant. Equipment observations from dual-station laminators indicate that changing the anilox from a 60° hexagonal cell to a 45° tri-helical pattern reduces ribbing artifacts on the seal zone by improving coating thickness uniformity to within ±0.25 g/m². The refined web is converted into cocoa powder sachets, tea overwrap, and microwave popcorn bag inner ply where a burst strength above 20 kPa is mandatory.

    Cementitious repair mortars prescribed under EN 1504-3 for structural class R3 or R4 frequently incorporate a VAE redispersible powder or liquid dispersion to bridge static and dynamic cracks up to 0.3 mm width. When SUMIMKAFLEX S-456HQ is substituted as a liquid modifier in a polymer-to-cement ratio (p/c) of 0.08–0.12 by solid weight, the mixing water is reduced by the water content of the emulsion so that the overall water-to-cement ratio stays within 0.38–0.42. The calcium hydroxide-rich pore solution initially destabilizes the latex particles, but the ethylene segments in the copolymer backbone resist complete saponification and during hydration form a continuous interpenetrating network that raises the flexural strength to 8–11 MPa and the direct tensile bond strength to concrete substrates above 1.5 MPa when tested per EN 1542. A typical production sequence involves a 250-litre forced-action pan mixer charged with Portland cement (CEM I 42.5 R), silica sand 0–2 mm, and cellulose ether (0.05% on dry mass), followed by the premixed liquid phase containing S-456HQ and a defoamer based on polyether siloxane, mixed for 180 s at 45 rpm. Field application failures observed with competitive non-carboxylated VAE grades include surface crusting in sunny conditions, which reduces open time below 15 min; S-456HQ’s colloidal stabilization maintains a workable consistency for 30–40 min at 35°C ambient. The end-use products include low-sag vertical repair mortars, polymer-modified waterproofing slurries for concrete balconies tested under EN 14891, and cement-based tile adhesives meeting ISO 13007-1 classification C2S1.

    Glass transition temperature shifts in air-laid nonwoven binder saturation directly modulate cross-machine direction tensile uniformity.

    Air-laid webs destined for flushable wipes, absorbent cores, and disposable medical drapes are bonded through a saturation process where SUMIMKAFLEX S-456HQ is diluted to a solids content of 16–22% and applied on a wire-mesh belt at a pick-up ratio of 80–120% relative to fiber dry weight. The specific Tg of S-456HQ, near 0°C as determined by differential scanning calorimetry per ISO 11357-2, imparts a flexible, non-blocking film that avoids the papery noise associated with styrene-acrylic binders. The controlled rewetability is critical: the surfactant package co-dried with the emulsion must yield a water-contact angle that drops below 50° within 3 s for flushability without causing premature disintegration during warehousing in tropical climates where humidity reaches 90% RH. Entirely distinct from wet-laid systems, the foam bonding variant—using a Foam-Mix head that aerates the binder to a density of 150–250 g/L—demands a foam half-life exceeding 120 s, a property that S-456HQ maintains when tuned with 0.5–1.0% ammonium stearate. Conformity to EDANA/INDA NWSP 360.1 for metal content and to the OEKO-TEX Standard 100 Annex 6 for skin-contact Class I articles is documented for lot-specific certificates. The converting line downstream of the saturation dryer—typically stretching 18 m with four heating zones 110/130/140/125°C—delivers rolled goods for baby wet wipes, hospital underpads, and biodegradable plant mulching mats where elongation at break exceeds 300% in the machine direction.

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    Certification & Compliance
    More Introduction
    A vinyl acetate-ethylene copolymer dispersion for high-solids, low-VOC adhesive and coating formulations, SUMIMKAFLEX S-456HQ is an anionic-stabilized aqueous emulsion with a nominal solids content of 55 ± 1 wt%, a pH of 4.5–5.5, and a Brookfield RV viscosity of 800–2,000 mPa·s at 25°C (spindle #4, 20 rpm). The product exhibits a minimum film-forming temperature below 0°C without external coalescent and a mean particle size of 1.5 µm as measured by laser diffraction. Its polymer backbone incorporates 18–22 wt% ethylene, which depresses the glass transition temperature of the amorphous phase to approximately −20°C (DSC, second heat) and confers permanent tack even on low-surface-energy substrates. Unlike conventional VAE grades where elevated ethylene content is achieved at the expense of cohesive strength, S-456HQ retains a gel fraction above 40% in tetrahydrofuran after 24-h extraction, indicating a lightly crosslinked architecture introduced during emulsion polymerization via a post-added organosilane-functional monomer. In continuous high-speed lamination of transparent packaging films, wetting of corona-treated low-density polyethylene remains the rate-limiting defect source. With a surface tension of 31–33 mN/m post-treatment, LDPE requires a dynamic wetting speed that exceeds line speeds of 200 m/min. When a comparative standard VAE with 14% ethylene was applied through a reverse-gravure coater at a coat weight of 2.5 g/m² (dry), adhesive-to-film contact angle hysteresis above 10° was recorded at 180 m/min, resulting in micro-foaming at the nip. In contrast, the same test run with S-456HQ—applied from a 52% solids bath with a viscosity of 1,200 mPa·s—yielded stable dynamic contact angles below at 220 m/min, attributed to its higher macromolecular mobility at processing temperature. Peel strength on flexible packaging polypropylene, evaluated per ASTM F904, increased from 0.9 N/15 mm for the low-ethylene VAE to 2.7 N/15 mm for the S-456HQ laminate after 7-day curing at 23°C/50% RH. Cohesive failure within the tissue layer, rather than interfacial delamination, was the predominant failure mode in T-peel testing (ASTM D1876).

    What Limits Shelf-Stability in High-Solids VAE Emulsions During Tropical Storage?

    Formulations based on S-456HQ are typically stored and shipped in IBC containers without nitrogen blanket, but uncontrolled headspace oxygen can initiate slow radical propagation at residual double bonds when ambient temperatures exceed 40°C. Real-time monitoring in a Jakarta warehouse (ambient 34°C, 95% RH) over 12 months revealed a viscosity drift of +150 mPa·s per month for a sample stored in an HDPE container, while the same batch stored in a steel drum with epoxy lining exhibited +30 mPa·s per month. This differential is traced to iron-mediated peroxide decomposition catalyzed by trace metal ions leaching from unlined carbon steel at pH values below 5.0. Unlike polyvinyl alcohol-stabilized VAE systems, which often build yield stress due to syneresis, the anionic surfactant shell of S-456HQ maintains colloidal stability largely independent of soluble polymer depletion flocculation. Nonetheless, pre-filtration through a 100-µm bag filter is recommended immediately before application if the emulsion has been stored with > 10% ullage for more than 90 days at temperatures exceeding 30°C.

    Crosslinker Compatibility and Post-Cure Performance in Textile Laminates

    Textile-to-textile bonding of polyester nonwovens using S-456HQ alone yields dry tensile strength adequate for temporary assembly (4.2 MPa, ASTM D751), but exposure to 60°C water for 1 h reduces bond strength to 0.8 MPa due to plasticization of the amorphous ethylene-rich phase. The inclusion of a water-dispersible aliphatic polyisocyanate at 1.5 wt% on emulsion solids elevates the wet tensile strength to 3.5 MPa under identical conditions. However, pot life becomes critically short: viscosity doubles within 45 min at 23°C when an HDI-trimer crosslinker is added under high-shear disperser agitation. By switching to a heat-activated blocked isocyanate dispersion (de-blocking onset 120°C) and blending via a static mixer immediately before slot-die application, a 6-h working window is achieved with no detectable gel particle formation. The system cures fully in 90 s at 150°C impingement oven temperature, producing a crosslink density of 2.4 × 10⁻⁴ mol/cm³ (calculated from equilibrium swelling in toluene using Flory-Rehner theory). Commercial acrylic binders used for the same application require 140°C for 180 s to reach comparable wet-resistance performance, giving S-456HQ a productivity advantage in fabric finishing lines where dwell time in the oven is the bottleneck. When formulating pressure-sensitive adhesives for transparent removable labels on glass, the common failure mode is ghosting—residual adhesive left behind after peel. This is exacerbated when the adhesive’s storage modulus at the peel temperature falls below the Dahlquist criterion of 3 × 10⁵ Pa. Dynamic mechanical analysis of a neat S-456HQ film at 1 Hz shows a storage modulus (G′) of 4.8 × 10⁵ Pa at 25°C and 1.2 × 10⁵ Pa at 60°C. To lift the high-temperature modulus without sacrificing tack, post-addition of a hydrogenated rosin ester dispersion (acid number 8 mg KOH/g, softening point 100°C) at 20 phr shifts G′ to 2.3 × 10⁵ Pa at 60°C while maintaining loop tack on glass at 3.2 N/25 mm (ASTM D6195). The resulting adhesive is clean-removable from float glass after 72 h at 40°C, showing less than 5% area coverage by adhesive residue when inspected under UV light at 365 nm. A competitive waterborne acrylic PSA of similar loop tack left 23% residue under the same protocol.

    A parametric comparison with solvent-free acrylic and standard VAE emulsions

    The following data contrasts film and adhesion properties of S-456HQ against a high-solids acrylic emulsion (Tg −30°C, 50% solids) and a low-ethylene VAE (Tg +5°C, 55% solids), all tested as single-component films without crosslinker.
    PropertyTest MethodS-456HQStandard VAE (low E)Acrylic Emulsion
    Film Mechanics
    Tensile Strength (MPa)ISO 37 (Type 2)8.212.49.7
    Elongation at Break (%)ISO 379403101,260
    100% Modulus (MPa)ISO 370.93.80.6
    Adhesion to LDPE at 23°C
    180° Peel Strength (N/25 mm)ASTM D3330 (Method A)5.31.82.1
    Failure ModeVisualCohesive (film)Adhesive interfaceMixed
    Emulsion Stability
    High-Shear Stability (min)ISO 13320 (at 5,000 rpm)>308>30
    Freeze-Thaw Cycles (−5°C/+25°C)Internal Method513

    The low modulus and high elongation of S-456HQ relative to low-ethylene VAE arise directly from the higher ethylene incorporation, which disrupts crystallinity in the vinyl acetate segments. The acrylic emulsion’s inherently broader molecular weight distribution yields higher extensibility but also a larger fraction of low-molecular-weight chains that plasticize at moderate temperatures, contributing to the inferior peel on non-polar LDPE.

    Regulatory Conformity and Volatile Organic Compound Profile

    S-456HQ is manufactured without the use of alkylphenol ethoxylate (APEO) surfactants and contains no intentionally added formaldehyde or formaldehyde donors. Its volatile organic compound content, determined by DIN EN ISO 17895:2024 (Method 1, boiling point up to 250°C), is 0.15 g/L. Key compliance standings are summarized below.
    Standard / RegulationScopeCompliance Status
    FDA 21 CFR 175.105Adhesives for indirect food contact (dry foods, incidental contact)Compliant
    EU 10/2011 and amendmentsPlastic materials and articles intended to come into contact with foodMigration limits met
    REACH (EC) 1907/2006Registration, Evaluation, Authorisation of ChemicalsAll substances registered for relevant tonnage bands
    RoHS 3 (2011/65/EU with 2024 amendments)Restriction of hazardous substances in electrical/electronic equipmentNot applicable to polymer, but all components assessed; no restricted phthalates or flame retardants
    German BfR Recommendation XXXVIPaper and board for food contactFree of constituents listed in anexes with SML exceeded
    In screen-printing of plastisol-free textile transfers, high-elongation waterborne adhesives often fail by re-emulsification under the hot-water wash test at 60°C specified in ISO 6330:2012. When S-456HQ was knife-coated onto a release paper at 100 g/m² wet and immediately nipped to a cotton fabric at 3 bar and 80°C, the cured composite withstood 15 home laundering cycles with dimensional change of the fabric below 1.5% and no visual delamination at the printed areas. This outcome exceeds the performance of a commercial low-Tg styrene-butadiene latex, which exhibited corner lifting after 8 cycles under identical conditions, attributed to a higher water absorption capacity of the SBR matrix. Pre-coating the S-456HQ layer with a thin (5 µm dry) ethyl vinyl acetate hot-melt adhesive via a slot-die lamination unit further boosted the wash resistance to 25 cycles without edge peel. When considering the substitution of solvent-borne polyurethane adhesives in footwear bonding, initial trials on SBR/leather joints demonstrated that S-456HQ alone cannot meet the 4.5 N/mm peel requirement at 50°C defined by SATRA TM411. A two-component construct, using a 2% addition of a polymeric hexamethoxymethyl melamine crosslinker catalysed with 0.3% p-toluenesulfonic acid (on solid weight), attained 4.8 N/mm after 8 min at 95°C heat activation. Production trials on a flat-bed press with a cycle time of 12 s at 110°C produced bonds exceeding 5.2 N/mm. A parallel trial using a medium-solids thermoplastic polyurethane dispersion required 70°C activation but exhibited a shelf-life pot of only 3 h once crosslinker was added, versus the 24 h working time recorded for the S-456HQ + melamine formulation. This long open time allowed operators to spread adhesive over 400 pairs per shift without cleaning mixing equipment between breaks, a critical ergonomic constraint in manual footwear adhesive application. For structural core-winding adhesives in paper tube manufacturing, water resistance must develop within the short distance between the glue station and the mandrel heat zone. A trial on a Model KT500 spiral tube winder operating at 45 m/min demonstrated that a blend of S-456HQ with 3% pre-gelatinized potato starch (dry-on-dry) formed a fibre-tearing bond on 200 g/m² kraft within 18 s at 120°C contact surface temperature. Tubes conditioned at 90% RH for 72 h retained 80% of their dry bursting strength (DIN EN ISO 2874). A conventional PVOH-stabilised VAE required 130°C and twice the dwell to reach similar humid burst retention, increasing energy consumption by 35% per linear metre. Any attempt to thicken S-456HQ with cellulosic ethers above a viscosity of 5,000 mPa·s should account for the risk of phase separation induced by the anionic emulsifier system. Alkali-swellable acrylic thickeners that rely on pH neutralisation above 7.5 will shift the emulsion pH into a range where acetate ester hydrolysis accelerates. A better route is the use of a nonionic associative polyurethane thickener at 0.05–0.2 wt%; this yields pseudo-plastic flow with a shear-thinning index of 0.25 (ratio of viscosity at 100 s⁻¹ to 1 s⁻¹), maintaining the homogeneity of the dispersion at temperatures as high as 50°C.