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Anhui Liwei Chemical Co., Limited.

SUMIMKAFLEX S-328HQ VAE Emulsion

    • Product Name: SUMIMKAFLEX S-328HQ 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 479016
    Appearance White milky liquid
    Solid Content 54-56%
    Viscosity 25 C Brookfield 1500-3500 mPa·s
    Ph 5.0-7.0
    Particle Size 0.5-1.5 μm
    Glass Transition Temperature Tg -14 °C
    Minimum Film Forming Temperature Mfft 0 °C
    Density 25 C 1.08 g/cm³
    Surface Tension 38 mN/m
    Ionic Character Nonionic
    Mechanical Stability Excellent
    Freeze Thaw Stability Good
    Wet Tack High
    Elongation At Break >800%

    As an accredited SUMIMKAFLEX S-328HQ VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in 200 kg drums, SUMIMKAFLEX S-328HQ VAE Emulsion is a water-based vinyl acetate-ethylene copolymer dispersion for adhesives.
    Container Loading (20′ FCL) 20′ FCL: SUMIMKAFLEX S-328HQ VAE Emulsion loaded in flexitanks or drums, securely palletized, container inspected, dry, clean, and stabilized for safe transit.
    Shipping Ship SUMIKAFLEX S-328HQ VAE Emulsion in sealed drums or IBC totes, protected from freezing and excessive heat. Not classified as dangerous goods for general transport, but avoid extreme temperatures to maintain stability. Ensure containers are secure, upright, and labeled properly to prevent leakage during transit.
    Storage Store SUMIMKAFLEX S-328HQ VAE Emulsion in its original, tightly sealed container in a cool, dry, well-ventilated area. Protect from direct sunlight and freezing. Ideal storage temperature is 5–35°C (41–95°F). Avoid exposure to excessive heat. Keep away from incompatible materials and sources of ignition. Use within the manufacturer’s specified shelf life to maintain product quality.
    Shelf Life Shelf life is six months from production date when stored in sealed containers at 5–35°C, protected from freezing and direct sunlight.
    Application of SUMIMKAFLEX S-328HQ VAE Emulsion
    ```htmlIn industrial wood bonding for interior load-bearing assemblies, the polymer dispersion is typically formulated into a one‑component adhesive with addition levels ranging from 78 wt% to 92 wt% of the total wet formulation, depending on the required open time and viscosity profile. Compliance with EN 204:2016 Durability Class D3 is achieved through controlled plasticizer migration and incorporation of polyvinyl alcohol as a protective colloid. The adhesive is applied via roller coater at a coat weight of 120–160 g/m² onto beech wood substrates conditioned to 12% ± 1% moisture content, followed by cold pressing at 0.8–1.2 MPa for 15–30 minutes and subsequent 7‑day conditioning at 23 °C/50% RH before shear testing. Terminal products include EN 12765‑classified kitchen chair seats, laminated stair treads, and three‑ply solid wood panels destined for interior furniture. On continuous roller‑coating lines running at 8–15 m/min, a critical failure mode emerges when the return roller picks up gelled particles from the pan: particle formation is suppressed only when mechanical stability, measured as < 0.3% coagulum on a 80 mesh screen after 5 min at 10,000 rpm in a laboratory dispermat, is maintained across the entire working day. Plant trials on a 4‑roll gluing spreader confirmed that batch‑to‑batch viscosity drift below 4000 mPa·s (Brookfield #4, 20 rpm) introduced foam rings at the doctor blade, whereas nitrogen-blanketed storage tanks and inline static mixers restored homogeneity without manual intervention.

    Why Does a Sub‑Zero MFFT Eliminate External Plasticizers in Recyclable Barrier Paper Coatings?

    Paper‑based food service packaging relies on a continuous polymer film to resist grease penetration and fibre swelling. When SUMIKAFLEX S‑328HQ is compounded at a dry addition rate of 12–18 parts per hundred of coating colour, the minimum film formation temperature of the neat dispersion measured at < 0 °C permits complete coalescence at room‑temperature drying without external coalescents, thereby maintaining direct compliance with FDA 21 CFR § 176.170(b) for components of paper and paperboard in contact with aqueous and fatty foods. The process employs an air‑knife coater on a 70–110 gsm bleached base paper at line speeds of 150–250 m/min; three‑zone drying at 80 °C, 110 °C, and 130 °C reduces residual moisture to below 2.5% before reel‑up. The resulting hot‑drink cups, sandwich wraps, and bakery bags exhibit Cobb60 values below 5 g/m² when tested per TAPPI T441 om‑21. A narrow processing window exists at coater solids exceeding 58%, where the rheology abruptly transitions from shear‑thinning to dilatant behaviour, generating transversal streaks visible under a 1000 lx inspection light; pre‑screening each batch with a controlled‑stress rheometer (cone‑plate 40 mm, shear sweep 0.1–1000 s⁻¹) identifies the critical solids threshold for a given pigment grade and dispersant level, allowing solids to be locked at 55% ± 1% where Brookfield viscosity holds between 800–1200 mPa·s (spindle #3, 20 rpm).The application of VA‑based binders to air‑laid and carded nonwoven webs for hygiene convertible products demands a balance between dry cohesion and peel‑off adhesion on silicone‑coated release liners. In a full‑scale converting trial on a 3‑card, 2‑beam nonwoven line producing 50 gsm polypropylene‑spunbond/composite cores, an impregnation bath concentration of 8% solids (diluted from the 55% stock emulsion with deionized water adjusted to pH 6.5–7.0) was metered by a kiss‑roller system leaving a wet add‑on of 35% ± 5%. The binder imparts a machine‑direction tensile strength of ≥ 22 N/50 mm after through‑air drying at 125 °C for 12 seconds, sufficient to withstand the ISO 9073‑3:1989 strip method for apertured coverstock intended as loop‑facing of hook‑and‑loop fastening tapes. Terminal articles encompass cotton‑blend wet wipes, incontinence brief backsheets, and disposable pillow protectors sealed with thermal‑bonded seams. Plant‑scale fluctuations arise when the web temperature entering the drying hood deviates by more than ± 4 °C: at 119 °C, residual 3.5% moisture trapped inside the binder film causes inter‑roll blocking on the calendar stack, while at 131 °C, the emulsion surface skins over prematurely, losing film continuity at embossing points. A non‑contact infrared sensor array controlling the hot‑oil temperature cascades within a ± 1.5 °C band proved mandatory for run lengths exceeding 8 hours.

    When Carpet Tile Delamination Strength Must Exceed 2.0 N/mm Under EN 14041

    Tufted carpet tile pre‑coat and secondary backing formulations incorporate the VA‑ethylene copolymer as a principal binder, typically at 45–65 dry parts per 100 dry parts of filler. Compounding is performed in a high‑dispersion, water‑cooled turbo‑mixer where the emulsion is blended with 350‑mesh calcium carbonate and an acrylic‑based thickener to reach a target viscosity of 18,000–25,000 mPa·s (#6, 20 rpm). The compound is applied via a lick‑roll applicator with an adjustable gap of 0.3–0.6 mm onto the backstitch of solution‑dyed nylon carpet, followed by fusing with a polyester nonwoven scrim and curing in a three‑pass flatbed oven with incremental zone temperatures of 100 °C/130 °C/150 °C. Delamination resistance requirements follow EN 14041:2018 Annex F, demanding ≥ 2.0 N/mm peel strength for contract‑use tiles installed over raised floors. Addition of 0.8–1.2 phr of a blocked isocyanate crosslinker raises the peel plateau to 2.5–3.0 N/mm after 48 h ambient post‑cure, but the crosslinker’s activation temperature of ≥ 135 °C mandates a minimum dwell time of 90 s in the final oven zone; any reduction in line speed below 4.2 m/min to compensate for slower heat transfer through the backing stack results in a measurable +0.8 unit increase in the b* yellowness coordinate (D65/10° spectrophotometer), rendering light‑coloured tiles outside the ΔE*a ≤ 1.5 shade tolerance. This trade‑off forces production scheduling to batch darker‑toned tiles on days when crosslinker‑containing recipes are run.

    Cementitious Waterproofing Slurries: Polymer‑to‑Cement Ratio and Capillary Pore Refinement

    Two‑component flexible cementitious waterproofing membranes for below‑grade retaining walls rely on the VA‑ethylene dispersion to bridge micro‑cracks. The liquid component is dosed at a polymer‑to‑cement ratio (p/c) of 0.08 by mass, corresponding to a polymer solids/cement ratio of 0.045, which when mixed with CEM I 52.5 N portland cement and 0.1–0.3 mm silica aggregate produces a slurry applied by notched trowel to a wet thickness of 1.5 mm. Curing under 23 °C/65% RH for 28 days yields a capillary water absorption coefficient of < 0.1 kg/(m²·h⁰˙⁵) as per EN 1062‑3:2008. Flexible‑grade membranes on precast concrete panels are tested to ASTM D638‑14 Type IV at 5 mm/min crosshead speed, showing an elongation at break of ≥ 35% and tensile strength retention of > 0.45 MPa after 5000 hours of QUV‑B accelerated weathering. When the p/c ratio is inadvertently raised above 0.12, the membrane retains excellent waterproofing but loses compressive strength beyond the EN 13813:2002 minimum of 12 MPa for levelling screeds, and adhesive tensile pull‑off from a dry concrete substrate drops to 0.3–0.5 MPa, below the 1.0 MPa threshold of EN 1542. Process‑wise, the open time of the slurry is limited to 23 minutes at 20 °C if the emulsion is not pre‑buffered; adding 0.2% (on emulsion) of a sodium gluconate‑based retarder extends pot life to 45 minutes without affecting the 1‑day compressive strength, enabling hand‑application on vertical surfaces with a sponge‑float finish. Finished membrane systems typically serve as tanking for elevator pits, internal wet‑room substrates, and protective interlayers beneath tile adhesive on external balconies.Flexographic printing of polyethylene shopping bags and industrial shrink wrap uses a water‑based ink in which the VA‑ethylene copolymer serves both as the pigment carrier and the primary adhesion promoter to low‑surface‑energy substrates. The let‑down vehicle is prepared by dosing the emulsion at 30–40% of the total ink weight into a pigment concentrate pre‑dispersed on a bead mill to < 5 μm fineness of grind. Corona‑treated low‑density polyethylene film with a surface energy of ≥ 40 dyn/cm is printed at 80 m/min on a 8‑colour central‑impression press equipped with ceramic anilox rollers of 180 l/cm line count. Curing under warm‑air knives at 55–65 °C results in blocking‑resistant surface within 2.5 seconds. Rub resistance per ISO 2836:2021 (Sutherland rub tester, 2‑pound weight, 200 cycles) must show ≤ 10% ink transfer, a value only attainable when the pH of the mixed ink is held between 8.2 and 8.8; above 8.9, amine‑vapor‑choaking in the drying hood fogs the operator’s field and triggers pH‑induced micro‑coagulation on the doctor blade. Ink stock stored in DI‑water‑rinsed totes for > 24 hours without mild agitation exhibits a skin layer that, when redispersed, generates visible pinholes in solid‑laydown areas > 15 cm²; hence, recirculation through a 60‑mesh in‑line basket strainer is mandated on press.
    Application‑referenced compliance matrix for SUMIKAFLEX S‑328HQ across six downstream domains
    Domain Primary Standard Test Method / Clause Typical Addition Critical Value
    Wood Bonding D3 EN 204:2016 Clause 6.2 / shear strength after cold water soak 80–92 wt% wet 2.0 MPa
    Barrier Paper Coating FDA 21 CFR 176.170(b) TAPPI T441 Cobb test 12–18 phr dry Cobb60 < 5 g/m²
    Nonwoven Bonding ISO 9073‑3:1989 MD tensile, 100 mm/min 8% bath solids 22 N/50 mm
    Carpet Tile Backing EN 14041:2018 Annex F, peel adhesion 45–65 phr dry 2.0 N/mm
    Cementitious Waterproofing EN 1062‑3 Capillary absorption p/c 0.08 w < 0.1 kg/(m²·h⁰˙⁵)
    Flexo Ink LDPE Printing ISO 2836:2021 Sutherland rub, 200 cycles 30–40% let‑down 10% transfer
    When the dispersion is co‑binder‑enhanced with 5–8% of a fully hydrolysed PVOH solution in gypsum‑based joint compounds, a dual‑setting mechanism emerges that governs feathering and sandability. Commercial knife‑grade formulations incorporate 2.5–3.5 wt% of the VA‑ethylene solids on total compound weight, blended under vacuum in a planetary mixer to 12,000–15,000 mPa·s (#7, 10 rpm) and applied via 12‑cm stainless‑steel taping knives onto paper‑faced tapered‑edge plasterboard. The VAE component reduces the water‑of‑convenience demand by 8% compared to all‑starch controls, while the calcium‑ion tolerance inherent to the carboxylated backbone prevents viscosity collapse when calcium sulphate hemihydrate hydrates exothermically; the peak temperature inside a 2 mm joint can reach 47 °C at 8 minutes after mixing, accelerating film formation but also risking mud‑cracking if the relative humidity falls below 35%. Meeting ASTM C475/C475M‑17 Clause 5.4 crack‑resistance and 5.6 bond strength requires post‑drying at 50 °C for 2 hours followed by conditioning at 75°F/50% RH to constant weight. Finished wall‑board seams, corner beads, and fastener heads decorated with latex‑based paints constitute the dominant end‑use, and any residual N‑methylolacrylamide from a non‑self‑crosslinking VAE grade would interact with the joint‑compound retarder, extending setting time beyond the 90‑minute working limit. Formulators therefore pre‑verify formaldehyde content to remain below 5 ppm in the compounded compound by EN 717‑3.
    Polymer‑to‑cement ratio effects on slurry properties in flexible waterproofing membranes (SMUD 0.1–0.3 mm sand, CEM I 52.5 N, 28d cure 23 °C/65% RH)
    p/c Ratio Compressive Strength ASTM C109 (MPa) Tensile Adhesion EN 1542 (MPa) Crack Bridging EN 1062‑7 (mm) Capillary Absorption EN 1062‑3 (kg/(m²·h⁰˙⁵))
    0.04 18.2 1.3 0.2 0.15
    0.08 14.6 1.1 0.6 0.07
    0.12 10.1 0.6 1.0 0.04
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    Certification & Compliance
    More Introduction

    SUMIMKAFLEX S-328HQ is an aqueous copolymer dispersion based on vinyl acetate and ethylene, produced by Sumitomo Chemical under the SUMIMKAFLEX trade name. The emulsion is characterized by a solids content of 55–57 %, a pH of 4.5–5.5, and a Brookfield LVF viscosity at 20 rpm, 25 °C in the range of 1800–3200 mPa·s. The ethylene content in the copolymer backbone, typically 18–22 wt% on dry polymer, yields a minimum film-forming temperature (MFFT) of 0 °C without external plasticizer, measured per ISO 2115. This internal plasticization distinguishes S-328HQ from conventional homopolymer PVAc dispersions and from VAE grades with ethylene levels below 12 %, which require coalescing solvents for film integrity below 7–10 °C. The particle size distribution, centered at 350–500 nm as determined by laser diffraction (ISO 13320), and the anionic surfactant stabilization system are optimized for high-shear mechanical stability in rotor-stator mixers and gear-pump transfer lines.

    When a Polyvinyl Alcohol Protective Colloid Is Not Sufficient

    Many VAE dispersions rely on polyvinyl alcohol (PVOH) as a protective colloid, which contributes to shear stability but often elevates surface energy and compromises wet adhesion to low-energy substrates. S-328HQ employs a mixed stabilizer package—a low-molecular-weight PVOH combined with a proprietary anionic surfactant—that depresses the dynamic surface tension to 36–38 mN/m at 1 ms bubble lifetime (maximum bubble pressure method, DIN 14370). On untreated polypropylene film, peel adhesion values measured per ASTM D1876 exceed 2.8 N/cm after 72 h conditioning at 23 °C, 50 % RH, whereas analogous PVOH-only grades register <1.2 N/cm. This performance gap widens under hot-humid conditions: after 7 days at 50 °C, 90 % RH, the S-328HQ bond retains 87 % of its original peel strength, while the PVOH-stabilized grade falls below 45 %. The mechanism is attributed to reduced interphase water uptake, with water contact angle on the dried film exceeding 82° versus 68° for traditional PVOH-protected types, limiting plasticization of the adhesive layer.

    Why Does S-328HQ Maintain Cohesion in High-Heat Laminating Processes?

    In roll-lamination of PVC edgebanding onto MDF panels, adhesive activation temperatures frequently reach 85–95 °C at the nip. Conventional VAE dispersions with ethylene domains that lack controlled crystallinity can undergo excessive softening above 70 °C, leading to bond slip and post-process delamination. S-328HQ integrates a sequence of ethylene-rich blocks that widen the melting endotherm; DSC scans (ASTM D3418) show a broad melting transition with a peak at 52 °C and a shoulder extending to 78 °C, maintaining a storage modulus G′ above 0.5 MPa at 95 °C as measured by DMA (1 Hz, 3 °C/min ramp). On a Barberán single-sided edgebander operating at 18 m/min with a hot-air activation nozzle temperature of 480 °C and a nip pressure of 0.4 MPa, the S-328HQ adhesive layer exhibits zero visible creep after 24 h under 1 kg dead load at 70 °C (EN 14257), while standard VAE types show 2–4 mm displacement. The formulation is free of added tackifier resins, eliminating the risk of phthalate or rosin-ester migration into PVC plasticizer systems.

    In waterborne contact adhesives for automotive interior lamination—specifically bonding PVC or TPO skins to ABS/polyolefin dashboard carriers—open time and immediate tack are critical. S-328HQ, when compounded with 3 wt% of a maleinized polybutadiene dispersion and 0.3 wt% of a fluorosurfactant wetting aid, provides a tack-free time of 6–8 min at 23 °C, 55 % RH, and 100 µm wet film thickness on a glass plate. The peak tack force, measured with a Polyken probe (ASTM D2979, 1 cm/s withdrawal), is 4.5 N. This open-time window is 2–3 min wider than that of standard VAE grades of similar solids, attributed to the controlled skinning rate afforded by the surfactant-latex architecture. During high-frequency welding of the finished laminate, the VAE film does not produce volatile chloride-releasing degradation products, confirmed by headspace GC-MS (VDA 278) showing <10 µg/g total VOC and <2 µg/g fogging condensate.

    Specifications and Comparative Data: S-328HQ Versus Conventional VAE Grades

    Key physical and performance parameters of SUMIMKAFLEX S-328HQ and a representative standard VAE dispersion (S-320)
    ParameterS-328HQS-320 (Standard VAE)Test Method
    Solids content55–57 %54–56 %ISO 3251
    pH4.5–5.54.0–5.0ISO 976
    Viscosity (Brookfield LVF, spindle 4, 20 rpm)1800–3200 mPa·s3000–6000 mPa·sISO 2555
    Ethylene content (dry polymer)18–22 wt%10–14 wt%FTIR internal standard
    MFFT0 °C4–7 °CISO 2115
    Dynamic surface tension (1 ms bubble)36–38 mN/m44–48 mN/mDIN 14370
    Dry-film water contact angle82–85°65–70°ASTM D7334
    Peel adhesion on PP (72 h, 23 °C)>2.8 N/cm1.0–1.5 N/cmASTM D1876
    Heat resistance (static load, 70 °C)Zero creep, 24 h2–4 mm creepEN 14257

    The S-328HQ viscosity profile is intentionally kept lower than typical cohesive grades to facilitate high-speed roller coating without the need for dilution water. In gravure coating operations at 80–120 m/min line speed with an open-pan doctor-blade system, the emulsion does not exhibit foaming above 0.5 vol% air entrainment even after 8 h recirculation, as measured by a density-based Foamalyzer at 40 °C.

    Film Formation in Humid Environments and the Problem of Water Spotting

    A persistent failure mode in woodworking adhesives based on VAE is the formation of white spots when condensed moisture contacts the dry bond line. These spots, visually objectionable on furniture edges, arise from localized re-emulsification of non-crosslinked PVOH domains. S-328HQ mitigates this through a controlled post-polymerization acetalization step using glyoxal, which consumes approximately 60 % of the available 1,2-diol sites on the PVOH stabilizer. The resulting film, after 7 days conditioning at 23 °C, 50 % RH, shows a water spot rating of 4–5 on the EN 12720 scale (cold water, 24 h), compared to 2–3 for untreated standard grades. In D3-class bonding tests (EN 204), the S-328HQ adheres to ash wood with a dry tensile shear strength of 14.5 MPa and maintains 7.8 MPa after 4 days cold-water immersion, well above the ≥2.0 MPa D3 minimum. The crosslinking chemistry does not introduce formaldehyde donors, and free formaldehyde content is below 5 ppm as verified by JIS A 1460 testing, making the emulsion suitable for F☆☆☆☆ registered applications.

    Stability Limitations and Incompatibility Boundaries

    The mixed stabilizer system of S-328HQ limits its tolerance for multivalent cations and strongly alkaline compounding ingredients. Addition of zinc oxide dispersions or calcium carbonate slurries above 2 phr can induce a viscosity rise exceeding 200 % within 24 h at 25 °C, with eventual gelation triggered by de-stabilization of the anionic surfactant component. Compounding is recommended within a pH window of 4.0–7.5; above pH 8.0, the ester linkages of the VAE backbone begin to saponify at a measurable rate, with a 0.5 % decrease in solids per month at 40 °C storage. In flooring adhesive formulations containing amine-epoxy co-reactants, the emulsion must be separated from the epoxy component until point-of-use, because amine accelerators cause premature acetal cleavage and embrittlement of the final film. When pre-drying of the applied wet film is required—particularly in relative humidity above 60 % and temperature below 15 °C—installation of an IR pre-gelling station with a surface temperature setpoint of 45–50 °C is mandatory to prevent water entrapment and subsequent interlayer blistering during hot-press lamination.

    Migratory Behavior in Low-VOC Carpet Backing Compounds

    Carpet tile manufacturing with bitumen or PVC plastisol secondary backings requires a pre-coat that does not soften or migrate into the reinforcing fleece during hot-press consolidation. S-328HQ, applied as a 200–250 g/m² dry pre-coat on polyester nonwoven, demonstrates <0.5 % mass loss by TGA isothermal hold at 150 °C for 2 h, indicating negligible volatile content after film formation. Under a 200 kN press at 140 °C for 15 min, the S-328HQ barrier layer prevents bitumen strike-through to the pile side, confirmed by cross-sectional SEM-EDX mapping showing no detectable sulfur (detection limit 0.1 wt%) above the pre-coat interface. In contrast, standard EVA-based pre-coats show a diffuse sulfur band extending 150–200 µm into the fleece, leading to pile-stiffening. The emulsion’s high ethylene content provides the necessary flexibility to pass the ISO 4918 artificial aging test with a tuft bind retention of >85 % after 5000 cycles of 60 °C heat-aging.