| HS Code | 471128 |
| Appearance | Milky white liquid |
| Solid Content | 55 ± 1% |
| Viscosity Brookfield 25 C | 500–2000 mPa·s |
| Ph | 6.0–7.5 |
| Glass Transition Temperature Tg | -20°C to -5°C |
| Particle Size | 0.1–0.3 μm |
| Minimum Film Forming Temperature Mfft | 0°C–10°C |
| Density | 1.05–1.10 g/cm³ |
| Residual Monomer | < 0.1% |
| Mechanical Stability | Good, no coagulum after centrifugation |
| Storage Stability | 6 months at 5–35°C |
| Peel Adhesion | Moderate to high |
As an accredited VAc-Acrylate Emulsion for Pressure Sensitive Adhesives factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in 200 kg drums, sealed polyethylene-lined steel containers, ensuring safe storage and handling of VAc-acrylate emulsion. |
| Container Loading (20′ FCL) | 20′ FCL: VAc-acrylate emulsion loaded in palletized drums/IBCs, secured, temperature-controlled to prevent freezing, with proper hazardous/transport documentation. |
| Shipping | VAc-Acrylate Emulsion is shipped as a non-hazardous aqueous dispersion in lined drums or IBC totes. Protect from freezing and excessive heat. Ensure secure containment to prevent leakage. Store upright, ventilated area. Standard chemical handling procedures apply; avoid skin/eye contact and follow local transport regulations for safe delivery. |
| Storage | Store VAc-Acrylate Emulsion in tightly sealed, original containers in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Maintain temperatures between 5–35°C; do not allow freezing. Keep away from strong oxidizers and acids. Stir gently before use, and follow shelf-life guidelines to prevent coagulation or degradation. |
| Shelf Life | Shelf life: 12 months from production date when stored sealed, cool, and frost-free. |
On a stretched BOPP carton sealing line running at 1,200–1,600 m/min, the practical upper coating speed for a compounded VAc-acrylate emulsion PSA is governed by residual moisture removal from the transfer-coated adhesive, not by substrate tensile stability. The adhesive is reverse-roll coated onto a siliconised release liner at a wet film thickness that yields 18–22 g/m² dry adhesive, dried through a four-zone hot-air tunnel with zone setpoints of 70 °C, 90 °C, 110 °C, and 105 °C, and then laminated to corona-treated BOPP film at a surface energy of 38–42 dyn/cm. A production formulation uses 100 wet parts of the base VAc-acrylate dispersion at 54–56% solids, 10–20 dry parts of rosin ester tackifier dispersion per 100 dry parts polymer, 0.2–0.5 parts of dioctyl sulfosuccinate wetting agent per 100 wet parts, and 0.05–0.20 dry parts of polyurethane associative thickener per 100 dry parts polymer to bring coatability to 300–600 mPa·s at 25 °C. On high-speed slitting lines, stringing failure occurs when the wetting agent exceeds 0.6 parts or when the blade temperature exceeds 40 °C; adhesive transfer to the backing is observed when unwind tension is kept above 1.8 N/mm for 48 mm rolls. Finished rolls of 48 mm and 72 mm nominal width are evaluated under ASTM D3330/D3330M for 180° peel, ASTM D6195 for loop tack, and ASTM D3654/D3654M for static shear; adhesive layers intended for indirect food-contact package closure are assessed under FDA 21 CFR 175.125, and REACH Article 33 declarations are triggered when SVHC content exceeds 0.1% w/w in the imported article. Terminal product types include brown carton sealing tape, transparent office-grade tape, and heavy-duty bundling tape used on corrugated export cartons.
Viscosity drift during transfer coating is a major process variable when the emulsion is compounded at a converter rather than supplied as a precompounded grade. The addition of rosin ester tackifier dispersion raises the wet viscosity from a typical base value of 300–800 mPa·s to 600–1,200 mPa·s depending on the tackifier particle size and pH after ammonia adjustment; when the pH rises above 8.0, the emulsion develops a dilatant response under the high shear of a comma coater, leading to edge spatter. The coated liner is dried to residual moisture below 0.5% by Karl Fischer titration before lamination; residual moisture above 1.0% lowers the subsequent shear adhesion on BOPP and creates microvoids that appear as silver streaks in the adhesive layer. Batch-to-batch variance in the base emulsion particle size, typically between 220 nm and 280 nm, alters loop tack and requires compensating coat-weight adjustment on the coating head.
| Standard designation | Property measured | Test condition |
|---|---|---|
| ASTM D3330/D3330M | 180° peel adhesion | Stainless steel panel, 24 h dwell, 300 mm/min |
| ASTM D6195 | Loop tack | Loop speed 305 mm/min |
| ASTM D3654/D3654M | Static shear holding power | 1 kg load, 25 mm × 25 mm bonded area |
| FDA 21 CFR 175.125 | Pressure-sensitive adhesive suitability | Indirect food-contact package closure |
Removable paper and film labels convert cleanly only when the VAc-acrylate emulsion is formulated with a low peel-to-shear ratio and coated within a narrow window of 12–18 g/m² dry. Below 12 g/m², edge lift occurs on low-energy substrates such as polyethylene board; above 18 g/m², adhesive transfer and facestock tear rise after 60 days on polypropylene surfaces. The laboratory test used to catch residue is FINAT FTM 21 peel from glass at 300 mm/min and FINAT FTM 9 loop tack, while the production check uses a 90° peel from stainless steel after 24 h dwell. A formulation for removable paper labels uses 100 wet parts of VAc-acrylate PSA base, 5–12 dry parts of ester tackifier per 100 dry parts polymer, 0.1–0.3 parts of ammonium hydroxide to maintain pH 7.0–8.0, and 0.05–0.15 parts of mineral-oil defoamer. In the coating plant, the emulsion is applied to a 62 µm silicone release liner by a slot die at 250–350 m/min, dried in three zones to residual moisture below 0.5%, and laminated to paper or polypropylene facestock. Rotary die cutting at 120–180 cuts/min generates dust and edge stringing if the adhesive fails to reach a plateau shear storage modulus above 1 × 10⁵ Pa at 25 °C; production trials on roll-fed machines show batch-to-batch peel variance of ±0.4 N/25 mm when the base emulsion particle size shifts from 220 nm to 280 nm. Terminal product types include A4 laser labels, logistics box-end labels, and removable beverage glass labels. The relevant food-contact framework for labels used on food packaging is Regulation (EC) No 1935/2004, with the adhesive layer subject to EU 10/2011 when a functional barrier is not demonstrated.
From a rheological perspective, removable label formulations are adjusted so that the dynamic strain sweep at 1 Hz gives a crossover frequency between 0.1 rad/s and 1 rad/s; if the crossover is below 0.05 rad/s, the adhesive remains too elastic and produces high striations during die cutting. The coat weight is monitored on-line by beta gauge or infrared scanning; deviation of ±1 g/m² across the web is tolerated for general-purpose labels but not for freezer-grade removable labels, where cold-temperature adhesion loss is evaluated after 24 h at −20 °C. Coating lines running at 350 m/min require a machine-direction web tension below 0.6 N/mm after lamination to prevent facestock curl and silicone release liner buckling.
Transfer of a low-Tg VAc-acrylate emulsion to corona-treated LDPE masking film requires a dry adhesive deposition of 5–12 g/m² to keep aged peel force below 0.5 N/25 mm on polycarbonate and ABS sheet. The coating operation uses a five-roll reverse gravure station at 120–200 m/min, with in-line corona treatment of the substrate at 40–44 dyn/cm and oven temperatures limited to 60–80 °C to prevent film distortion. The formulated adhesive contains 100 wet parts VAc-acrylate base, 2–6 dry parts hydrogenated rosin ester per 100 dry parts polymer, 0.1–0.3 parts nonionic acetylenic diol surfactant, and 0.2–0.4 parts high-molecular-weight polyether defoamer; the batch is mixed under vacuum at 15–20 m/s tip speed for 10–15 minutes to remove fish eyes. High-shear mixing above 25 m/s is avoided because it reduces the emulsion particle size distribution stability and increases foam generation. The adhered film is tested by ASTM D3330/D3330M 180° peel at 300 mm/min, ASTM D6195 loop tack, and ISO 6270-2 condensation resistance after 7 days at 40 °C/90% RH; on production trial coils, adhesion build-up on injection-molded polycarbonate panels from 0.3 N/25 mm to 0.8 N/25 mm after 14 days at 50 °C is considered a rejection criterion. Stress whitening and adhesive transfer appear above 0.8 N/25 mm when the film is removed from polished PC, especially if the film is stretched during application. Terminal product types include laser guard film for acrylic sheet, polyethylene masking film for polycarbonate glazing, and coextruded surface protection film for stainless steel panels during bending and punching. The composition must avoid amine-based pH adjusters; ammonia is preferred because amine addition above 0.2 parts can produce yellowing on polycarbonate after 14 days of UV exposure. Compliance documentation includes REACH Annex XVII, RoHS recast 2011/65/EU, and California Proposition 65 if residual vinyl acetate exceeds the practical analytical detection threshold.
For optically demanding protective films, the VAc-acrylate emulsion is selected for a particle size below 250 nm to avoid stress whitening on polished surfaces; batch-to-batch shifts in mean particle size from 220 nm to 280 nm lower tack and require line speed compensation. The wetting agent and defoamer package is validated by a foam collapse test, where a 100 mL sample after 5 min high-speed dispersion must return to less than 5 mL foam within 15 min; otherwise pinholes appear on LDPE film. Coating trial records show that peel force on low-energy polypropylene rises from 0.2 N/25 mm to 0.6 N/25 mm after 30 days at 23 °C when the tackifier level is increased by 2 dry parts per 100 dry parts polymer, which requires a corresponding reduction in dry coat weight for peel-sensitive applications.
Because ISO 10993-10 cytotoxicity testing of finished medical laminates is performed on aqueous extracts, residual vinyl acetate monomer in the dried VAc-acrylate PSA is treated as a release endpoint, with typical supplier specifications at or below 50 ppm in the wet dispersion and 10 ppm after drying. The VAc-acrylate emulsion chosen for skin-contact applications is formulated without alkylphenol ethoxylates and without amine-based pH adjusters; a typical wet blend contains 100 parts of the base medical-grade dispersion, 0.3–0.7 parts of a polyfunctional aziridine crosslinker per 100 dry parts polymer to lower extractables, and 0.1–0.3 parts of a silicone-free defoamer. The adhesive is slot-die coated at 25–35 g/m² dry onto a 25 µm polyurethane film, a perforated polyethylene film, or a nonwoven backing, then dried in three zones at 50 °C, 70 °C, and 90 °C and crosslinked at 70–80 °C for 24–48 h before die cutting. When run on a 12-head rotary die cutter at 80–100 cuts/min, adhesive ghosting on the liner increases if the wet emulsion viscosity falls below 800 mPa·s at 25 °C; conversely, viscosity above 2,000 mPa·s produces starved transfer and coating streaks. Terminal device types include ECG electrode fixation rings, ostomy flange tapes, wound dressing border adhesives, and wearable sensor patches. Compliance testing is performed under ISO 10993-5:2009 for cytotoxicity, ISO 10993-10:2010 for skin irritation and sensitization, and ISO 10993-1:2018 for biological evaluation planning; published data for the correlation between crosslinker addition and skin-specific irritancy for this VAc-acrylate grade is limited, so converter validation under ISO 10993-10 is required before commercial device assembly. The adhesive is not indicated for direct wound contact when residual vinyl acetate monomer in the dried film exceeds 10 ppm, and it is not combined with polyvinylpyrrolidone-based hydrogels because soluble PVP migrates into the PSA and reduces shear holding power.
In ECG electrode conversion, the adhesive is coated on a 125 µm PE release liner before transfer to nonwoven or foam substrates, and the laminated web is slit at 50–80 m/min. A persistent failure mode is oozing at the die-cut edges when the coat weight exceeds 35 g/m² or when the crosslinker is added below 0.3 parts; edge oozing after sterilisation is evaluated by visual inspection under 10× magnification. The adhesive is compatible with ETO and gamma sterilisation for terminal products, but gamma irradiation above 25 kGy may increase crosslink density and reduce initial tack, so dose mapping is required for each reel lot; published data for gamma dose tolerance of this specific VAc-acrylate grade is limited.
Ultra-clear overlaminate films demand that the dried VAc-acrylate adhesive layer maintain optical clarity and peel stability after accelerated UV exposure. The adhesive is formulated with 100 wet parts VAc-acrylate PSA base, 0.1–0.2 parts of a nonionic wetting agent, 0.05–0.15 parts of a polysiloxane-free defoamer, and 0.03–0.08 parts of a UV absorber per 100 wet parts when outdoor weatherability is specified. No rosin ester tackifier is used in this scenario because tackifiers with aromatic content raise haze above 1.5% on 50 µm PET facestock. The adhesive is slot-die coated at 15–20 g/m² dry onto optically clear PVC or PET, dried at 70–90 °C, and laminated under 20–60 N/cm roll pressure. The finished overlaminate is tested by ASTM D1003 for total transmittance and haze, ASTM D3330/D3330M for 180° peel on glass, ASTM D3654/D3654M for static shear at 1 kg, and ISO 4892-3 for UV-A fluorescent weathering after 500 h. On production rolls, entrapped air bubbles and mottling are controlled by wetting agent surface tension below 32 mN/m at 0.2 parts; lower surface tension may cause dewetting on silicone release liners. Terminal products include cold lamination films, floor graphic overlaminates, window graphic films, and vehicle wrap overlaminates. Compliance documentation for EU market placement includes REACH Article 33 SVHC communication and, for PVC substrates, RoHS recast 2011/65/EU where the end laminate enters electronic display applications.
Lamination condition is critical: if the coated film is routed through an orientation zone above 110 °C, the adhesive can undergo post-crosslinking and develop gel particles; process temperature is therefore capped at 90 °C in the drying oven. Haze is measured on a 50 µm PET carrier after the adhesive is laminated to 80 µm PVC; a haze rise from 0.8% to 1.5% after 500 h UV-A testing indicates photo-oxidation and is used as a batch rejection line. The same test matrix applies to cold lamination films used in architectural graphics, where reworkability requires clean removal from glass after 30 days at room temperature without adhesive residue.
| Standard designation | Property measured | Test condition |
|---|---|---|
| ASTM D1003 | Haze and luminous transmittance | 50 µm PET after lamination |
| ASTM D3330/D3330M | 180° peel adhesion | Glass panel, 24 h dwell, 300 mm/min |
| ASTM D3654/D3654M | Static shear | 1 kg load, 25 mm × 25 mm area |
| ISO 4892-3 | UV-A fluorescent weathering | 500 h, 50 °C black panel |
In low-VOC automotive interior lamination lines, the VAc-acrylate emulsion is used as a waterborne contact adhesive for bonding open-cell polyurethane foam to polyolefin backing sheets, with dry coat weights between 30 g/m² and 50 g/m² applied by roll or spray equipment. The compounding ratio for this application uses 100 wet parts of the VAc-acrylate dispersion, 2–8 dry parts of a stabilized ester tackifier per 100 dry parts polymer, 0.2–0.4 parts of a polyurethane thickener per 100 wet parts to maintain 1,000–2,500 mPa·s at 25 °C, and 0.1–0.3 parts of a mineral-oil-free defoamer. The wet adhesive is applied to the polyurethane foam by a two-roll coater or a 0.8–1.2 mm nozzle spray system, forced-air dried at 50–70 °C for 2–5 minutes, and bonded under 2–4 bar laminating nip pressure. Failure in production is most often observed as foam strike-through when the wet adhesive viscosity drops below 800 mPa·s, or as edge curling when the dry coat weight exceeds 50 g/m². The laminated parts are tested by VDA 278 for VOC and fog emission, VDA 270 for odour, and ISO 6452:2021 for fogging; the adhesive layer is specified as low-emission and is not formulated with free formaldehyde donors or aromatic solvents. Terminal product types include door panel inserts, instrument panel skin attachments, headliner edge wraps, and seat back pockets. The main limitation is plasticizer migration from PVC skins, which reduces shear holding power after 500 h at 85 °C and requires additional crosslinking for vinyl-bonded assemblies.
Spray application stations on door panel lines use 0.8–1.2 mm nozzle orifices at 4–6 bar atomising pressure; lower pressure produces wet droplets that penetrate open-cell foam and increase foam strike-through. The foam substrate is dried to below 0.5% moisture before adhesive application because residual water reacts with the ester tackifier and causes pH drift. The final laminate is held at 23 °C/50% RH for 72 h before VDA 278 testing to allow any residual ammonia to volatilise. Batch records show that when the tackifier level exceeds 8 dry parts per 100 dry parts polymer, the laminate develops a measurable odour increase under VDA 270 and is rejected for visible interior applications.
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Vinyl acetate–acrylate copolymer emulsions for pressure-sensitive adhesives are aqueous dispersions of a random copolymer produced by semi-continuous emulsion polymerization. The model VAcA-PSA 4015 uses a monomer mixture in which vinyl acetate is 30–40 wt% and n-butyl acrylate is 55–65 wt%, with 1–5 wt% acrylic acid and 0.2–0.6 wt% n-dodecyl mercaptan as molecular weight regulator. The dispersion is anionically stabilized and buffered with sodium acetate; solids are controlled at 54–56%, viscosity at 250–450 mPa·s by Brookfield RVT spindle 3 at 20 rpm and 25 °C, and pH at 4.5–5.5 per ISO 976. Intended uses include transfer-coated and direct-coated paper and film labelstock, splicing tapes, and removable protective films. The product differs from all-acrylic PSAs by lower raw-material cost and higher polar adhesion to unprimed poly(ethylene terephthalate) and polyvinyl chloride; from styrene-acrylic emulsions by lower aromatic content and better tack on low-energy films; and from solvent-borne acrylic PSAs by the absence of flammable solvent handling and lower volatile organic compound content. In comparison with ethylene–vinyl acetate hot melts, it provides room-temperature pressure-sensitive behaviour without heated melt application.
Because the product is a colloidally stabilized dispersion rather than a solution, freeze-thaw stability and shear stability are handling constraints. The dispersion is not freeze-thaw stable without propylene glycol; exposure to -5 °C causes irreversible grit formation. The product is supplied with biocidal protection that meets ISO 11930 preservation criteria under challenge testing; validation is site-specific. Rheology and adhesive properties are strongly dependent on the degree of carboxylic acid neutralization. At pH below 4.2, mechanical shear stability under a high-speed disperser test is reduced; at pH above 6.0, the dispersion can exceed 600 mPa·s and wetting on corona-treated polyethylene drops. Industrial coating operations adjust pH with ammonia to 5.0–5.3 before addition of thickeners or tackifier dispersions; failure to control this range is a reported batch-to-batch source of die-line defects in slot-die coating.
In a VAc-acrylate PSA, cohesive strength is governed by gel architecture, polymer molecular weight distribution, and drying-side crosslinking. Vinyl acetate homopolymer has a glass transition temperature near +32 °C, while poly(n-butyl acrylate) is approximately -54 °C; a 35:65 VAc:nBA random copolymer therefore exhibits a Fox Tg near -28 °C. This places the plateau storage modulus in the 104–105 Pa range at 23 °C, which is appropriate for pressure-sensitive adhesion but lower than the 105–106 Pa plateau of an all-acrylic copolymer containing methyl methacrylate. The lower plateau modulus increases room-temperature tack but reduces high-temperature shear.
In static shear at 70 °C and 1.0 kg with a bonded area of 25 mm × 25 mm on stainless steel per ASTM D3654/D3654M, films of VAcA-PSA 4015 cast at 25 g/m² dry coat weight fail cohesively in 8–24 h. An all-acrylic control with similar loop tack typically exceeds 48 h under the same conditions. The difference results from chain transfer to the acetate methyl group during radical polymerization, which broadens molecular weight distribution and limits the very high molecular weight fraction that resists shear. Crosslinking with aluminum acetylacetonate or a polyfunctional aziridine at 0.3–0.8 wt% on dry polymer raises gel fraction to 45–60%, measured as tetrahydrofuran insolubles. If gel fraction exceeds 65%, loop tack on high-density polyethylene falls below 6 N/25 mm in ASTM D6195, so the formulation is constrained by the tack-shear envelope.
Polymerization is run as a starved-feed semi-batch at 75–80 °C with a persulfate-bisulfite redox initiator. The feed of acrylic acid is staged during the final 20% of monomer addition to locate carboxyl groups on the particle surface and improve colloidal stability; if acrylic acid is fed uniformly, carboxyl groups bury in the particle and viscosity stability on storage worsens. This is observed on a 2,000 L production reactor as viscosity drift of +100–200 mPa·s over 30 days at 30 °C. Increasing vinyl acetate content from 30 to 40 wt% raises 180° peel on stainless steel by approximately 1.5–2.0 N/25 mm and lowers static shear at 70 °C by 30–50%. Formulation adjustments with acrylic acid above 5 wt% increase crosslink density but reduce tack on low-energy surfaces; below 1 wt% shear stability and cohesive strength are insufficient.
For incoming raw-material control and release testing, the dispersion is characterized by the parameters in Table 1. Solids content is determined by ISO 3251:2019 using 2.0 g sample mass dried at 105 °C for 3 h. Viscosity is measured after 24 h conditioning at 25 °C; values below 250 mPa·s may indicate under-neutralization or high residual water from distillation, while values above 450 mPa·s may indicate coagulum or excessive alkali. Residual vinyl acetate is monitored by headspace gas chromatography; free monomer above 0.1 wt% changes odour classification and may affect compliance under REACH and the aqueous dispersion volatile organic compound limits. Minimum film-forming temperature is tested according to ISO 2115; typical values of -16 to -12 °C permit coalescence without high-boiling coalescent at substrate surface temperatures above 5 °C. The dispersion is shear-stable when passed through a 25 µm screen; retained coagulum above 50 mg/L is treated as a batch rejection because it produces die lines in slot-die coating.
| Parameter | Test method | Typical range / limit |
|---|---|---|
| Appearance | Visual inspection | White, homogeneous |
| Solids content | ISO 3251:2019 | 54–56% |
| pH | ISO 976 | 4.5–5.5 |
| Viscosity | Brookfield RVT, spindle 3, 20 rpm, 25 °C | 250–450 mPa·s |
| Minimum film-forming temperature | ISO 2115 | -16 to -12 °C |
| Particle size | ISO 22412 dynamic light scattering | 180–320 nm |
| Residual vinyl acetate | Headspace gas chromatography | ≤0.1 wt% |
| Density | ISO 2811-3 | 1.02–1.06 g/cm³ |
| Coagulum on 25 µm screen | Internal method | ≤50 mg/L |
Batch-to-batch viscosity variation is most sensitive to pH adjustment and defoamer addition. In production, raising pH from 4.7 to 5.2 with ammonia increases Brookfield viscosity by 80–120 mPa·s. At pH 5.8 or above, microflocculation can increase 25 µm screen retention from <50 to >120 mg/L within 72 h, a failure mode observed in summer storage above 30 °C. Filtration through 25 µm bags is recommended before slot-die coating to protect the die lip.
The dispersion is pseudoplastic and thixotropic. At 25 °C and shear rate 10 s⁻¹, apparent viscosity is 300–500 mPa·s; at 1,000 s⁻¹, it falls to 80–140 mPa·s, which is low enough for slot-die transfer coating without high-pressure pumps. A pilot comma coater with 1.2 m web width and a lip gap of 150–250 µm applies 90–110 µm wet film at 12–18 m/min to give 22–28 g/m² dry coat weight on 23 µm silicone-coated PET liner. Drying uses two zones: 70–80 °C for 3 min followed by 100–110 °C for 2 min. Wet film thickness above 120 µm produces skin-over blistering on air-impingement dryers because surface coalescence occurs before water flux through the film is complete. This is a production limitation that caps line speed when dry coat weight is increased.
Thixotropic recovery time is relevant to transfer-coating processes with short open times. After shear at 1,000 s⁻¹ for 60 s, viscosity recovers to 80% of the low-shear value within 30–60 s; a recovery time above 90 s causes leveling defects in comma-roll coating because the wet film remains fluid after lamination. Foam is controlled with 0.1–0.3 wt% of a non-ionic defoamer added under low-shear mixing at 20–40 rpm; high-shear incorporation above 1,000 rpm can break the dispersion and raise coagulum. Surfactant migration from rewetting operations lowers loop tack by more than 15% because a hydrophilic surfactant layer forms at the adhesive-air interface. Dynamic surface tension at 100 ms bubble life should remain below 45 mN/m; values above this indicate insufficient wetting on release liner and can produce cratering in direct coating.
For transfer lamination, adhesive is dried on release liner and then nipped to a corona-treated facestock at 25–40 °C with nip pressure 3–6 bar. If lamination is attempted below 10 °C, the adhesive surface is too stiff and transfer is incomplete; if lamination is above 50 °C, film deformation may occur. On a production laminator with 1.3 m web width, a nip gap of 0.15–0.25 mm is used for 50 µm polypropylene facestock.
After 24 h dwell on stainless steel, dried films of VAcA-PSA 4015 at 25 g/m² on 50 µm polypropylene facestock show 180° peel adhesion of 10–13 N/25 mm according to ASTM D3330/D3330M. On high-density polyethylene, peel adhesion is 6–9 N/25 mm; on glass, loop tack is 8–12 N/25 mm by ASTM D6195. Static shear at room temperature with 1.0 kg on 25 mm × 25 mm stainless steel is 20–48 h; at 70 °C it drops to 8–24 h. These values place the material between a general-purpose all-acrylic emulsion and a styrene-acrylic emulsion in shear performance.
| Adhesive type | Peel adhesion on stainless steel (N/25 mm) | Loop tack on glass (N/25 mm) | Static shear 70 °C (h) |
|---|---|---|---|
| VAc-acrylate emulsion VAcA-PSA 4015 | 10–13 | 8–12 | 8–24 |
| All-acrylic emulsion | 11–15 | 10–14 | 48–96 |
| Styrene-acrylic emulsion | 7–10 | 6–9 | 30–60 |
| Solvent-borne acrylic | 13–16 | 12–16 | 100–200 |
The substitution of vinyl acetate for methyl methacrylate reduces hydrophobicity. White films of VAcA-PSA 4015 show visible water whitening after 24 h immersion at 23 °C; all-acrylic controls show less change. This limits unpigmented clear labelstock unless a clear acrylic overcoat or topcoat is applied. Tackifier compatibility is acceptable with rosin ester dispersions at 5–15 phr dry polymer; loop tack on polyethylene increases by 10–25%, but static shear at 70 °C decreases by 30–50%. Above 20 phr, shear falls below 4 h and the adhesive may leave residue on stainless steel. Plasticizer resistance differs from all-acrylic PSAs. After 7 days contact with dioctyl phthalate at 60 °C under 0.1 MPa, peel on stainless steel decreases by 15–25%, while an all-acrylic control may decrease by less than 10%. This limits use on plasticized PVC facestock unless a barrier liner or topcoat is applied.
For direct coating of VAcA-PSA 4015 onto corona-treated polyethylene, a surface energy of at least 40 mN/m is required, tested with dyne pens per ASTM D2578 within 2 h before coating. Treatment decay on low-density polyethylene can lower surface energy to 34 mN/m after 24 h, producing craters and non-uniform adhesive distribution. A wetting tension of 42–46 mN/m is preferred. The emulsion may be thickened with a polyurethane associative thickener to 800–1,200 mPa·s for direct gravure application. Thickening with cellulosic ethers above 0.5 wt% is not recommended because water-soluble polymer can bloom to the adhesive surface and reduce loop tack by more than 20% in ASTM D6195.
Coating at 20–25 g/m² dry weight on 30 µm polyethylene requires a first drying zone below 65 °C to prevent substrate shrinkage. Web temperatures above 75 °C cause dimensional loss and adhesive mottle. The dispersion is incompatible with high-valent cationic additives such as aluminum sulfate at pH below 4.5; contact causes instantaneous coagulation that cannot be reversed by shear. Storage in stainless steel or lined carbon steel vessels at 5–35 °C is acceptable; freezing below 0 °C is a boundary condition and causes irreversible grit formation. For indirect food-contact applications, the dried film may fall under FDA 21 CFR 175.105 when monomers and polymerization aids are compliant, but the converter is responsible for extraction validation under 21 CFR 177.1520 for olefin substrates.