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Anhui Liwei Chemical Co., Limited.

Celvolit 1319 VAE Emulsion

    • Product Name: Celvolit 1319 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 916359
    Product Name Celvolit 1319 VAE Emulsion
    Chemical Type Vinyl Acetate-Ethylene (VAE) Copolymer Emulsion
    Appearance White milky liquid
    Solids Content 55.0 ± 1.0%
    Viscosity 3000–6000 mPa·s (Brookfield, 20 rpm, 25°C)
    Ph 4.5–6.0
    Density Approximately 1.05 g/cm³ at 20°C
    Particle Size 0.5–2.0 μm
    Minimum Film Formation Temperature Mfft 0–5°C
    Glass Transition Temperature Tg Approximately -5°C
    Residual Vinyl Acetate Monomer <0.1%
    Freeze Thaw Stability Stable for up to 3 cycles
    Film Clarity Transparent, slightly hazy when dry

    As an accredited Celvolit 1319 VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Celvolit 1319 VAE Emulsion supplied in 200 kg steel drums or 1000 kg IBC totes for safe handling and storage.
    Container Loading (20′ FCL) 20′ FCL container loading of Celvolit 1319 VAE Emulsion uses flexitanks or drums, secured and stowed to prevent leakage and ensure safe transport.
    Shipping Celvolit 1319 VAE Emulsion is shipped as a non-hazardous aqueous polymer dispersion in drums, IBCs, or bulk tankers. Protect from freezing and excessive heat. Ensure containers are sealed, upright, and ventilated. Avoid contact with incompatible materials and follow standard safe handling procedures.
    Storage Store Celvolit 1319 VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Recommended storage temperature is 5–35°C; protect from freezing. Keep containers off the ground, avoid contamination, and use within six months of delivery for optimal performance.
    Shelf Life Shelf life is 12 months from manufacture date when stored in original sealed containers at recommended temperatures, protected from freezing.
    Application of Celvolit 1319 VAE Emulsion

    Formulated with Celvolit 1319 as the primary binder, aqueous adhesive systems for high-speed carton and multi-wall bag sealing typically incorporate a co-dispersed tackifier resin—most commonly a stabilized rosin ester emulsion at 10–25 parts per hundred dry VAE. Additive selection is governed by indirect food contact regulation FDA 21 CFR 175.105 and the European framework EU 10/2011 for specific migration limits. Production-scale application proceeds through engraved anilox rollers with cell volumes calibrated to deposit 2.0–4.5 g/m² dry weight at line speeds reaching 180–240 m/min. At these throughputs the wet tack development window must be shorter than 0.8 seconds to sustain splice integrity before the hot-air drying tunnel, which operates across four zones with ramp profiles from 85°C to 135°C at the final section. Failure modes observed on actual triple-wall corrugators: foaming if residual surfactant migration from the printed substrate exceeds 0.05 g/m², and fibre-tear loss when ambient humidity drops below 20% RH, causing too rapid skin-over. The finished bonded stock commonly converts into pharmaceutical secondary cartons, frozen-food overwrap and pet-food multi-wall sacks where the adhesive joint must resist -25°C cold-chain embrittlement without plasticizer leaching—verified by ISO 11339 T-peel at 23°C and -18°C. Low-temperature peel retention above 2.5 N/cm after 30-day ambient aging is regarded as minimum batch acceptance.

    Can Aluminium Chloride Post-Addition Unlock D3 Durability Without Pre-Cure Reactivity Instability?

    In type-II wood assembly adhesive compounding directed at EN 204/205 D3 classification, Celvolit 1319 is typically crosslinked with a buffered aluminium chloride solution dosed at 0.3–1.2 wt% of the liquid emulsion—calculated as AlCl3 hexahydrate on wet emulsion mass. The catalyst is introduced under high-shear mixing with a rotor-stator unit running at 2 800–3 200 rpm precisely 20–30 minutes before application, because the pot-life under ambient 23°C drops from over 8 hours to approximately 75–110 minutes when the Al3+ dosage crosses 0.9%. Process engineering on a continuous cold-press line demands inline viscosity monitoring through an oscillatory pipe rheometer; the moment real-part viscosity surpasses 18 000 mPa·s at 20 s⁻¹, the adhesive batch must be quarantined because gap-filling capability on uneven hardwoods (beech, ash) collapses.

    Open assembly time on a 40-gram/m² single-face spread averages 6–9 minutes at 55% RH, shrinking to 3.5 minutes when shopfloor temperature exceeds 30°C. Jigs are clamped at 0.6–0.9 MPa for 30–60 minutes and post-cured at ambient for 5 days before D3 water-resistance testing: 4 days cold water soak at 23°C, then immediate determination of wet tensile shear strength per ISO 6238, which must retain ≥ 2.5 N/mm² versus dry reference values typically in the 10–14 N/mm² bracket. An industrial hazard arises when beech substrates with inherent acidity below pH 4.8 prematurely chelate the aluminium, causing a matt-chalky bondline with >40% wet-strength loss. End-user applications include kitchen-chair tenon dowelling, laminated stair treads and acoustic guitar rim assembly, all requiring DIN EN 12765-conformant bond integrity under intermittent temperature excursions to 80°C as verified by the D4 boil test cycle.

    Lamination Peel Hierarchies in Air-Laid Nonwoven Cores

    When Celvolit 1319 is deployed as a sprayable binder in tiered absorbent hygiene cores, the emulsion is first diluted to 18–22% solids with deionized water and combined with a non-ionic alcohol ethoxylate wetting agent at 0.15–0.35% on wet weight to reduce dynamic surface tension below 34 mN/m at 100 ms surface age. Spray-bar systems with 0.25 mm-orifice hydraulic nozzles atomize the liquor at 1.8–4.0 bar onto a pre-formed fluff-pulp/SAP blend travelling on a 2.5-metre-wide forming wire at 120–220 m/min. Instantaneous wetting onto cellulose is critical; if the contact angle exceeds 15° after 50 ms, pin-holing develops across the absorbent pad, visible as irregular dry-bond pockets under UV-dye inspection. Following the spray zone, a through-air drum set at 145–165°C dries the matrix to below 3% residual moisture in 4–7 seconds, after which inline peel testing per ISO 9073-4 at 90° angle confirms target delamination resistance between 0.6 and 1.1 N/25 mm.

    Regulatory compliance for infant diapers mandates a skin-sensitization assay following OECD 406 and migration of formaldehyde below the 16 µg/g detection limit—Celvolit 1319’s self-crosslinking groups evolved during drying must not generate detectable aldehyde residues in the finished web. A documented route to low-peel failure occurs when the SAP fraction exceeds 45 wt% of the core; the high-swelling gel particles mechanically disrupt the binder bridges upon saline contact, driving the wet peel below 0.2 N/25 mm. To circumvent this, a two-pass “print bond” pattern with gravure rollers applying 1.5 g/m² additional VAE at the SAP-rich zones is implemented, raising wet integrity to above 0.55 N/25 mm as measured after 10-minute immersion in 0.9% saline at 37°C. The finished structures are converted into ultra-thin incontinence pads and premium diaper acquisition-distribution layers where fluid-handling properties coexist with structural cohesiveness.

    How Does Filler Loading Beyond 70% Affect Loop Backing Anchorage?

    In tufted broadloom and automotive carpet manufacturing, the pre-coat compound is formulated by charging a high-shear planetary mixer with Celvolit 1319 and then incrementally feeding ground calcium carbonate with a particle size cut of D50 ≤ 5 µm until the filler-to-binder dry ratio reaches 1.8:1 to 3.2:1 (equivalent to 64–76 wt% filler on total dry weight). At the 76% threshold a sharp rise in Casson yield stress from 12 Pa to 48 Pa is recorded using a cone-and-plate rheometer, signalling that transfer pump cavitation may occur if the paste is not conditioned through a vacuum de-aeration vessel operating at –0.85 bar gauge. The compound is knife-over-roll coated onto woven polypropylene or polyester primary backing at 500–800 µm wet thickness to encapsulate the tuft stitches; anchoring performance is quantified post-cure by tuft-withdrawal force according to ASTM D5843, with 4.1–6.6 N for nylon 6.6 two-ply loop configurations as the contractual range for commercial-tile backings.

    A persistent line problem arises from the hydrolysis-sensitive nature of the primary backing sizings: if the VAE pre-coat pH drifts above 7.8 after filler incorporation, alkaline attack on the polypropylene’s organosilane lubricant strip leads to 21–28% loss in edge-ravel resistance within 14 days of warehouse ageing. Therefore, a pH buffer of 0.15% sodium acetate is stirred in once the pre-coat passes through a colloid mill. The secondary lamination with a styrene-butadiene foam or a polyurethane gel requires that the VAE pre-coat develop a minimum surface energy of 38 mN/m after plasma treatment; inline Dyne-test pass/fail acceptance at 42 mN/m is applied immediately upstream of the foam mixer. Finished carpet modules achieve ISO 2551 dimensional stability with ≤ 0.15% shrinkage after steam conditioning and can carry Cradle-to-Cradle Gold certification when the VAE backbone contributes to a halogen-free regime in post-consumer debonding.

    When Portland Cement/VAE Slurries Demand Open-Time Extension Beyond 90 Minutes

    In two-component polymer-modified cementitious waterproofing slurries—commonly specified for balcony, bathroom and planter applications under GB/T 23445-2009 Type II or EN 14891 membrane systems—Celvolit 1319 is used as the liquid polymer constituent blended with a dry-mix powder containing 42.5R white Portland cement, 70–100 mesh silica sand and a polycarboxylate superplasticizer at 0.15% of binder weight. The standard liquid-to-powder ratio by weight is set at 1:2.8, yielding a fresh mortar with a flow cone time of 30–35 seconds per EN 13395-1. Because the VAE acrylic-free composition must deliver a crack-bridging ability of ≥ 0.75 mm at –10°C, the polymer-cement ratio (p/c) calculated on solids is raised to 0.18–0.24, pushing the dry film elongation above 200% per ASTM D412 Die C.

    Performance shift with polymer-cement ratio in JS membrane formulations
    p/c (solids)Water absorption after 24 h (%)Flexural strength 28 d (MPa)Adhesion 28 d (MPa)Crack bridging at –10°C (mm)
    0.1012.47.10.80.21
    0.186.25.51.30.54
    0.243.94.11.80.82

    Applying the slurry by roller or trowel in two to three coats to achieve a dry film thickness of 1.5–2.0 mm demands an extended open time because retouching of cementitious gels formed after 70–80 minutes can disturb film integrity and reduce final bond strength. VAE helps keep the initial Vicat needle penetration depth above 30 mm for 95–110 minutes at 20°C/65% RH, which is a 35% improvement over purely acrylic-modified batches. Nevertheless, on-site quality control must keep the liquid component above +7°C during storage and mixing; below that threshold coalescence is incomplete and micro-crazing appears under an optical microscope at 100x after 7‑day fog-box cure. The waterproofing systems find end-use in underground parking ramps, tiled wet-room substrates and concrete tank linings where adhesion after 7-day water immersion—measured by pull-off per EN 1542—must stay above 1.0 MPa.

    Dispersal coating of recycled linerboard with Celvolit 1319 diluted to 38–42% solids extends water-resistance measured by Cobb 1800-second test (ISO 535) to values below 22 g/m² while preserving full repulpability under the LAG 11/97 procedure of the Confederation of European Paper Industries. Air-knife metering sets the wet coating weight at 5.5–8.0 g/m² on a size-press running at 650 m/min. The coated sheet exits the after-drying section at 4.5% moisture and curbside-recyclable fast-food clamshells, fruit-tray dividers and agricultural transport crates are the dominant commercial conversions. An incompatibility arises with optical brightening agents of the stilbene-triazine class, whose quenching effect reduces the Hunter whiteness index by 3–5 points at 1.2 g/m² brightener loading. To hold brightness above 80° ISO, mills substitute a benzooxazole derivative and maintain the first nip pressure at 22 kN/m. Process slip during extremely humid summers (condensate film on cold rolls) can scatter the Cobb values by ±4 g/m²; inline infrared edge-driers operating at 4.2 kW/m are retrofitted as a remedy.

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    Certification & Compliance
    More Introduction
    Celvolit 1319 is a surfactant-stabilized, water-based vinyl acetate-ethylene (VAE) copolymer dispersion manufactured by Celanese. The product is supplied as a free‑flowing, milky‑white liquid with a solids content determined by ISO 3251 of 54–56 % by mass. Under standard shear conditions (Brookfield RVT, spindle 4, 20 rpm, 23 °C), the dynamic viscosity falls in the range 1 000–3 000 mPa·s as measured per ISO 2555. The pH (ISO 976) is maintained between 4.0 and 5.0, imparting an anionic character compatible with a broad range of formulation adjuncts. Minimum film‑forming temperature (MFFT) determined according to ISO 2115 is typically 0 °C, eliminating the need for external coalescing agents under most ambient application conditions. The dispersion contains no alkylphenol ethoxylate (APEO) surfactants, no intentionally added formaldehyde or formaldehyde‑releasing agents, and complies with the chemical restrictions of EU Ecolabel and Nordic Swan criteria for indoor paints and adhesives.

    How do the built‑in cohesion and plasticizer‑free flexibility of Celvolit 1319 influence D3 wood adhesive durability?

    In D3 interior wood assembly adhesives tested under EN 204, the primary performance demand is retention of bond strength after 4 h immersion in cold water. Celvolit 1319, with an ethylene comonomer content between 10 and 15 % by weight of the polymer backbone, provides permanent internal plasticization that reduces the glass‑transition temperature to approximately −15 °C. This low‑Tg architecture avoids the migration and eventual embrittlement observed with monomeric plasticizers such as dibutyl phthalate or benzoate esters. In a standard beech‑block D3 test assembly (glue spread 150 g/m² double‑side, open time 8–10 min at 23 °C/50 % RH, cold press 0.7 N/mm² for 30 min), the neat dispersion yields wet tensile strengths consistently exceeding 2.0 N/mm² after the 4‑h soak, provided the wood moisture content is controlled between 8 and 12 % prior to gluing. For applications requiring D4 durability (boil‑resistant), a post‑addition of a water‑dispersible polymeric isocyanate crosslinker at 5–10 % by weight of the dispersion is common. The pot‑life of such a two‑component system at 23 °C is limited to 90–120 min; batch sizes must therefore be matched to throughput on panel‑press lines with throughput capacities below 500 panels/h. On a Becker‑van Hüllen short‑cycle press with a platen temperature of 80 °C and a press time of 120 s, the crosslinked adhesive achieves D4 pass criteria with a 24‑h cold‑soak wet tensile strength above 4.0 N/mm² and a delamination rate below 5 % on three‑ply spruce laminations. Formulators should note that the isocyanate reacts preferentially with water; therefore, pre‑mixing must be conducted under controlled relative humidity (≤60 %) and the mixed adhesive must be used before a Brookfield viscosity increase of 30 % is observed.

    Long‑open‑time packaging adhesives and hot‑tack development

    Polymer‑dispersed paper and packaging laminations require a balance between extended open time on high‑speed roll‑coating lines and rapid hot‑tack formation under heated nip pressure. Celvolit 1319, owing to its small average particle diameter of approximately 1.5 µm (laser diffraction, ISO 13320) and a unimodal size distribution, deposits uniformly on cellulose substrates without excessive penetration into the sheet. On a Bachofen‑type three‑roll coating station running at 80 m/min with a gravure cylinder of 45 lines/cm, a wet film weight of 12–15 g/m² is achieved without misting. The low MFFT and high wet‑tack plateau of 0.6–0.8 N/25 mm (as determined by a Texture Analyser using a 25 mm probe, compression 2 N for 5 s) enable the adhesive to hold polyethylene‑coated board in place within 2 s of nip closure at 70 °C. Compared with homopolymer poly(vinyl acetate) dispersions of equivalent solids, Celvolit 1319 exhibits a lower heat‑seal activation temperature—the temperature at which cohesive strength reaches 1.0 N/25 mm is reduced by approximately 10–12 °C. This is attributable to the ethylene segments facilitating chain entanglement under mild thermal activation. The consequence is a broader processing window on blister‑pack sealing machines (e.g., Uhlmann BEC 300), where dwell times can be shortened from 1.5 s to 0.8 s without sacrificing seal integrity. It should be noted that prolonged exposure of the wet adhesive film to ambient conditions (open time > 30 min at 25 °C/45 % RH) leads to a measurable drop in hot‑tack due to skinning; line speed adjustments are necessary when intermittent stops exceed 15 min. Incorporation into cementitious tile adhesives (C2TE classification per EN 12004) requires careful attention to the dispersion’s anionic charge and its interaction with high‑pH, calcium‑rich slurries. Celvolit 1319 is typically added at 3–7 % on cement weight to a dry‑mix composed of CEM I 42.5 R, silica sand (0.1–0.5 mm), and cellulose ether (0.3–0.5 %). The polymer particles coalesce during the drying phase and form a continuous network that improves tensile adhesion strength after water immersion, fulfilling the ≥ 0.5 N/mm² requirement stipulated by EN 12004 for C2 adhesives. However, alkalinity‑induced saponification of the acetate groups is a known degradation pathway; long‑term wet‑storage tests (EN 1348) reveal that tensile adhesion values can decline by 15–20 % after 28 days under permanent immersion at 23 °C if the formulation pH exceeds 12.5. Buffering the mortar with a pozzolanic additive such as metakaolin (5 % of cement weight) helps maintain pH below 12.2 and preserves wet adhesion above 1.0 N/mm² after 28‑day immersion.
    Typical specification data for Celvolit 1319 VAE emulsion
    PropertyValueTest method
    Solids content54–56 %ISO 3251
    pH4.0–5.0ISO 976
    Brookfield viscosity (RVT, spindle 4/20 rpm, 23 °C)1 000–3 000 mPa·sISO 2555
    Minimum film‑forming temperature0 °CISO 2115
    Density at 20 °C~1.07 g/cm³ISO 2811-1
    Particle size (d50)~1.5 µmISO 13320
    Residual monomer (vinyl acetate)< 0.1 %GC headspace method
    Emulsifier systemAPEO‑free, anionic/non‑ionic

    When formulating low‑emission interior wall primers, what role does the absence of coalescing agents play?

    Interior primer formulations governed by AgBB or CDPH Standard Method v1.2 impose strict TVOC limits of 100 µg/m³ after 28 days in emission test chambers (ISO 16000‑9). Because Celvolit 1319 has an MFFT of 0 °C, coalescing solvents such as texanol, butyl glycol, or dipropylene glycol n‑butyl ether can be entirely omitted down to application temperatures of 5 °C. In a model formulation containing 25 % pigment volume concentration of titanium dioxide (rutile, 0.3 µm), 40 % Celvolit 1319 on total formulation weight, and calcium carbonate filler, the total volatile organic content (TVOC) as determined by ISO 11890‑2 is below 1 g/L. The wet scrub resistance (ISO 11998) after 200 cycles shows a film loss of < 5 µm, indicating sufficient film integrity without the need for supplementary film‑forming aids. Nevertheless, the absence of coalescent presents a risk of crack formation when applied at high wet‑film thicknesses exceeding 300 µm under forced drying at 40 °C and 15 % RH. Under these conditions, surface skinning occurs within 3 min, and microscopic film contractions appear as mud‑cracking. Recommended maximum wet‑film build is 250 µm per coat, with a minimum inter‑coat interval of 4 h at 23 °C/50 % RH. Airless spray application through a 0.015 inch tip at 120 bar yields acceptable spray patterns without cobwebbing, provided the emulsion has been diluted with 5–8 % water by weight to lower the high‑shear viscosity to 100–150 mPa·s (cone‑and‑plate, 10 000 s⁻¹).
    Contrast with adjacent Celanese VAE and PVAc grades
    GradeChemistryEthylene contentMFFT (°C)Typical use emphasis
    Celvolit 1319VAE, APEO‑free10–15 %0Balanced cohesion/flexibility for D3 wood, packaging, cement
    Celvolit 1350VAE, APEO‑free~18 %< −3Very high flexibility, low‑temperature adhesive, high wet tack
    Celvolit 1325VAE, carboxylated~13 %0Improved adhesion to metals, alkali‑resistance in cementitious coatings
    Celvolit 203PVAc homopolymer0 %+18High stiffness, D2 wood, requires plasticizer for flexible films
    Differences between Celvolit 1319 and a higher‑ethylene analogue such as Celvolit 1350 become evident in tensile testing (ISO 527‑3, film dried 7 days at 23 °C/50 % RH). The 1319 film exhibits a tensile strength of 4–5 MPa and an elongation at break of 300–400 %, while Celvolit 1350 with its greater ethylene content drops to a tensile strength of 2–3 MPa but extends to 600–700 % elongation. For joint‑sealing tapes or textile laminates requiring high deformation without cohesive failure, the higher‑ethylene grade is preferred; for load‑bearing wood bonds where dimensional stability under creep is critical, Celvolit 1319 provides superior resistance to time‑dependent shear deformation. Operational boundaries must be rigorously observed during storage and handling. The dispersion must be protected from freezing; if frozen and then thawed, irreversible coagulation and a rise in screen residue (retained on a 40 µm filter) above 1 % are expected. Storage temperature should be kept between 5 °C and 30 °C. Pump transfer should employ low‑shear equipment—progressive cavity pumps with rotational speeds limited to 200 rpm and stator elastomers compatible with the mildly acidic pH—to avoid shear‑induced grit formation. When used in conjunction with inorganic pigments such as iron oxides, a preliminary compatibility test is advisable: a blend of 90 % dispersion and 10 % pigment paste, stirred for 5 min at 1 000 rpm, should show a viscosity rise no greater than 500 mPa·s and remain free of grain upon draw‑down with a 100 µm applicator. Compliance with FDA 21 CFR §175.105 permits incorporation of Celvolit 1319 in adhesives intended for indirect food contact (packaging of dry foodstuffs), provided the finished adhesive film is separated from the food by a functional barrier. For use in indirect food‑contact paper coatings, migration testing under the relevant simulant (e.g., Tenax® for dry foods, EN 1186‑13) must confirm overall migration below 10 mg/dm². The dispersion also meets the volatile organic compound requirements of the European Decopaint Directive (2004/42/EC) for the “Primers” subcategory (limit 30 g/L VOC for water‑borne products, phase II). Not every ambient‑cure application benefits from Celvolit 1319. When the substrate is a low‑surface‑energy polymer such as untreated polypropylene or polyethylene, a surface treatment to raise the dyne level above 38 mN/m is necessary; the neat dispersion will not wet surfaces with surface energies below this threshold. In contrast, a carboxylated VAE such as Celvolit 1325 may provide marginal adhesion improvement on some metals, but published data for this specific configuration is limited. In pressure‑sensitive adhesive (PSA) constructions where a permanent tack is required, the neat dispersion does not yield sufficiently high probe tack (typically < 0.2 N/25 mm) and must be compounded with tackifying resin dispersions (e.g., rosin ester dispersion at 10–20 % on dry polymer). On a pilot coater running a release‑liner PSA transfer process at 15 m/min, a modified formulation containing 15 % tackifier dispersion and 0.5 % associative thickener produced a dry coat weight of 20 g/m² with a loop tack (FINAT FTM 9) of 3.5 N/25 mm, acceptable for removable decal applications. The tackifier-loaded system, however, exhibits a measurable drop in shear adhesion failure temperature (SAFT) from 120 °C (neat) to approximately 80 °C, limiting its use in hot‑fill label scenarios.