| HS Code | 529674 |
| Appearance | Milky white liquid |
| Solid Content | 55 ± 1% |
| Viscosity Brookfield 25 C | 1000-3000 mPa·s |
| Ph | 4.5-6.5 |
| Glass Transition Temperature | -5°C to 5°C |
| Minimum Film Forming Temperature | 0-5°C |
| Particle Size | 0.5-2.0 μm |
| Density 25 C | 1.05-1.10 g/cm³ |
| Ethylene Content | Medium (approx 15-25% by weight) |
| Residual Vinyl Acetate Monomer | <0.1% |
| Freeze Thaw Stability | Stable up to 3 cycles |
| Mechanical Stability | Good |
As an accredited Medium Ethylene VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Medium Ethylene VAE Emulsion is packaged in 200 kg drums or 1,000 kg IBC totes, sealed to prevent contamination. |
| Container Loading (20′ FCL) | 20′ FCL container loading of Medium Ethylene VAE Emulsion uses flexitanks or drums, ensuring secure stowage, leak prevention, and balanced weight distribution. |
| Shipping | Medium Ethylene VAE Emulsion is typically shipped as a non-regulated aqueous polymer dispersion in drums, IBCs, or tank containers. Protect from freezing and keep above 5°C to prevent coagulation. Avoid strong oxidizers. Proper shipping name: “Polymer Emulsion” (not hazardous) unless residual monomer levels require classification. |
| Storage | Store Medium Ethylene VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and freezing conditions. Maintain temperatures between 5°C and 40°C. Keep containers upright to prevent leakage, and avoid contact with strong oxidizers. Use within recommended shelf life, stirring gently before use if separation occurs. |
| Shelf Life | Shelf life is typically 6–12 months when stored sealed, protected from frost, and kept at moderate temperatures. |
In a production-scale water-based laminating adhesive for BOPP-to-metalized PET and paper-to-foil structures, medium ethylene VAE emulsion is selected when the converting line cannot tolerate solvent recovery and requires wetting on nonpolar film surfaces corona-treated to 38–42 dyn/cm. The grade is characterized by an ethylene monomer content of 10–20 wt%, reducing film hardness and enabling adhesion to LDPE and aluminium foil without a separate primer. Compounding uses 65–85 wet parts of a 50–55% solids dispersion per 100 parts liquid adhesive, equivalent to 35–47 dry parts VAE solids; final Brookfield viscosity is adjusted to 2,500–4,000 mPa·s at 25 °C with a polyvinyl alcohol protective colloid. Compliance for incidental food-contact use is documented under FDA 21 CFR 175.105, and European converters require a Declaration of Compliance under Regulation (EC) No 1935/2004; residual vinyl acetate monomer is controlled below 1,000 ppm and verified by gas chromatography before sale into food-packaging laminates. In the coating department, direct gravure or two-roll coating deposits 2.0–3.5 g/m² dry coat weight onto the primary web; the laminate then passes through a heated nip at 60–80 °C and a forced-air drying tunnel at 120–150 °C for 3–5 s. The emulsion must remain colloidally stable under recirculating pump shear, and pH is therefore buffered to 4.5–5.5 with 0.05–0.10 wt% sodium bicarbonate; drift above 6.0 produces overnight viscosity climb and gravure streaking. Terminal finished structures include snack-bar wrappers, lidding films, stand-up pouches, and paper/aluminium peelable lidding where fibre-tear bond strength is required after 24 h at 23 °C and 50% RH.
On a 500 kg stainless-steel mixing vessel, batch-to-batch viscosity drift is controlled by pre-dispersing the protective colloid for 30 min before emulsion addition; pH is corrected with dilute ammonium hydroxide rather than sodium hydroxide because sodium ion levels above 200 ppm can reduce wetting on corona-treated film. High-shear stability is monitored by a Hamilton Beach high-shear mixer at 3,000 rpm for 30 min; viscosity loss above 5% triggers rejection of the batch for gravure supply. During drum-transfer operations, progressive cavity pumps are operated below 150 rpm and 0.5–1.0 bar inlet pressure to prevent cavitation and microfoam formation. Amine-based defoamers are restricted to 0.1 wt% because residual amine can raise pH above 6.0 and destabilize the emulsion overnight. Cold-seal adhesive variants using the same medium ethylene VAE grade require a separate heat-resistance verification on the specific paper/foil structure, as published data for peel strength under tropical warehouse cycles is limited and must be generated on the customer’s film.
Formulating an interior flat wall paint with medium ethylene VAE emulsion typically requires 20–30 wet parts of a 55% solids dispersion per 100 parts total formulation, providing 11–17 dry parts binder solids and placing the dry film in a 55–75% pigment volume concentration range. The medium ethylene content lowers minimum film formation temperature to 0–5 °C, allowing coalescent demand to remain below 2 wt% of binder solids while still forming a continuous film at 10 °C and 60% RH. Production-scale pigment dispersion is carried out on a Cowles high-speed disperser at a tip speed of 18–22 m/s for 20–30 min, after which the VAE emulsion is added during letdown with a propeller agitator below 3–5 m/s to avoid shear-induced coagulation. Final pH is adjusted to 8.0–9.0 with 0.1–0.3 wt% 2-amino-2-methyl-1-propanol; overdosing above 0.5 wt% contributes free amine to VOC measurements and can depress wet scrub resistance. North American formulation registrations use ASTM D2486 scrub testing with a specification of at least 400 cycles before failure for commodity interior flats, ASTM D3960 VOC determination below 50 g/L, and ISO 11998 wet-scrub classification for EU retail chain reporting. The finished products include interior ceiling and wall flat paints, low-odour primer-sealers, and contractor-grade airless spray emulsions.
| Standard/Code | Parameter | Interior Flat Specification |
|---|---|---|
| ASTM D2486 | Scrub cycles to failure | ≥ 400 cycles |
| ASTM D3960 | VOC content less water and exempt solvents | < 50 g/L |
| ISO 11998 | Wet-scrub resistance classification | Class 2 or better |
| EU Directive 2004/42/EC | Maximum VOC content, water-based interior matt wall and ceiling paint, category A/a | 30 g/L |
Failure modes observed in high-volume architectural tint lines include viscosity drop following the addition of universal colorants because surfactant demand from the colourant can exceed the stabilization capacity of the emulsion; formulators typically pre-disperse colorants at 2–4 oz/gal and limit total colorant load to 12 oz/gal in medium ethylene VAE binders. Freeze-thaw exposure through three cycles from -5 °C to 23 °C without glycol or propylene glycol protection can create irreversible grit; therefore, winter-ready formulations use 5–10 wt% propylene glycol on total liquid paint. Application by airless sprayer with a tip size of 0.015–0.019 in at 1,500–2,000 psi yields acceptable film build, but pressures above 2,500 psi can shear the VAE dispersion and reduce scrub performance. Scrub failure in high-humidity bathrooms occurs when the dry film is exposed to condensation before 7 days cure, so maintenance cycles must specify full cure before water immersion.
Production of a two-component polymer-modified cementitious waterproofing slurry for basement tanking requires an emulsion that remains stable when mixed into cement paste with a pore solution above pH 12.5 and calcium ion concentration above 500 mg/L. Medium ethylene VAE emulsions are dosed at a polymer-to-cement mass ratio of 0.12–0.25, equivalent to 15–30 kg of a 50% solids dispersion per 100 kg of dry cementitious powder containing ordinary Portland cement, graded silica sand, and calcium formate accelerator. Compliance for liquid-applied water impermeable products is evaluated under EN 14891 for crack-bridging and adhesion, with additional certification under GB/T 23445 for polymer-cement waterproof coatings in export markets. Mixing on a double planetary mixer at 150–300 rpm for 3–5 min yields a lump-free slurry with flow table spread of 60–80 mm; pot life at 23 °C is 1–2 h, after which viscosity climbs more than 30% and loss of workability occurs. Application proceeds by notched squeegee or airless spray at 1.0–1.5 kg/m² per coat, giving dry film thickness of 0.6–1.0 mm; curing is maintained at 5–35 °C and 60–85% RH. Below 5 °C film coalescence stalls and the cured membrane may show tensile strength reductions greater than 50% relative to a 23 °C reference. Terminal products include balcony waterproofing under porcelain tile, wet-room tanking, concrete roof patches, and foundation retaining-wall membranes.
On multi-story shuttering lines, batch-to-batch variation in cement sand grading below 75 µm alters slurry rheology and can increase emulsion demand by 2–5 kg per 100 kg dry mix when fines exceed 35%; silo moisture above 0.5% should trigger re-qualification of the dry component. Spray equipment with a 4–6 mm reversible nozzle and 40–60 bar pump pressure provides adequate fan pattern, but longer hose runs above 30 m reduce working time because shear heating accelerates cement hydration. Over-watering during application, where site operatives add 5–10% water to extend pot life, violates mixing ratio and lowers membrane adhesion to below 0.5 MPa under EN 14891 pull-off testing; therefore, pre-weighed two-part kits are specified for quality-critical tanking work.
In carpet precoat and secondary-backing operations, the medium ethylene VAE emulsion is compounded with mineral filler to maintain a froth stability window that prevents foam collapse before oven gelation. The binder is added at 20–30 dry parts per 100 parts calcium carbonate filler, with total filler loading from 300–400 parts per 100 parts of binder solids; compound viscosity is held at 6,000–10,000 mPa·s at 25 °C with polyacrylate thickener. Emission compliance for finished carpet is verified under CRI Green Label Plus testing using ASTM D5116-17 small-chamber VOC methods and ISO 16000-6 sampling/analysis; VAE grades manufactured without formaldehyde-releasing biocides are specified to keep formaldehyde emissions low. In continuous froth application, an Oakes mixer operates at 1,500–2,500 rpm with metered air at 10–20 L/min to reduce specific gravity to 0.25–0.45; the froth is knife-coated onto secondary backing at 400–700 g/m² wet and passed through a three-zone forced-air oven at 120–130 °C, 130–140 °C, and 140–150 °C for 3–5 min total residence. Foam collapse before the first zone, or skinning above 150 °C, produces delamination and low tuft-bind strength in finished carpet. Terminal products include broadloom carpet with jute or polypropylene secondary backing, carpet tiles, and automotive floor mats.
Line-speed limitations appear when the oven exhaust humidity exceeds 60% RH, which retards water removal and forces a reduction from 25 m/min to 18 m/min to preserve full-film formation; burners and dampers are adjusted to maintain a negative pressure of 20–40 Pa in the first zone to avoid skinning. Precoat penetration into the primary backing is controlled by adjusting blade angle to 15–25° from vertical; excessive penetration increases hand stiffness and requires reprocessing. Viscosity drift during a production shift is monitored by rotational rheometer measurements at 1 s⁻¹ and 100 s⁻¹; a drop in low-shear viscosity below 5,000 mPa·s indicates thickener degradation and must be corrected before froth density exceeds 0.50.
When a nonwoven converting line shifts from styrene-acrylic to medium ethylene VAE binder for absorbent core wraps, the add-on level must be recalibrated because VAE softness and wet strength in low-odour hygiene structures differ from styrene-acrylic benchmarks. Binder solids are applied at 8–15 dry parts per 100 parts of cellulosic or bicomponent fibre, typically as a 12–20% solids sprayable dispersion, with residual moisture after drying maintained below 2%. Regulatory compliance for food-contact paper and nonwoven structures is established under FDA 21 CFR 176.170 for aqueous and fatty food-contact conditions, with EU REACH registration and BfR Recommendation XXXVI declarations required for European converter audits. On an air-laid drum former running at 200–400 m/min, the VAE dispersion is sprayed through air-atomizing nozzles at 1.0–2.5 bar and then dried in a through-air oven at 130–150 °C for 5–15 s. Production-scale bottlenecks occur when spray nozzles clog due to acidic VAE skin formation at pH below 4.0; buffering to 4.5–5.5 and using filtered feed pumps with 80–100 µm screen packs reduces downtime. Terminal finished products include absorbent core-wrap sheets, medical table drapes, wet wipes, and tissue laminates.
Publicly reported peel-strength variation across air-laid machine suppliers is limited, so each substrate must be validated on the specific former and through-air oven configuration before full production. Wet-strength retention after 60 min water immersion is evaluated by ASTM D5035 strip tensile to ensure the binder does not redisperse in the wet-wipe pack; values below 25% of dry tensile strength indicate undercure or pH drift. In hygiene converting plants, stock tanks are not left uncovered because atmospheric ammonia from nearby latex lines raises headspace pH and destabilizes the acidic VAE emulsion; closed-loop agitation at 10–20 rpm is sufficient for maintaining homogeneity without generating foam.
In blade-coated white-top kraft liner for cupstock and folding carton board, the high-shear rheology of the coating colour must remain below 120 mPa·s at 10,000 s⁻¹ while low-shear viscosity remains above 800 mPa·s; otherwise streaking and trailing blade defects appear at coating speeds of 600–1,200 m/min. Medium ethylene VAE emulsion is used as a sole or co-binder at 12–22 dry parts per 100 parts of kaolin and ground calcium carbonate pigment, with total coating solids held at 58–65%. For wet contact with food, the coated paperboard is evaluated under FDA 21 CFR 176.170 and FDA 21 CFR 176.180, while European buyers require a Declaration of Compliance under Regulation (EC) No 1935/2004 and BfR Recommendation XXXVI for paper and board. The coating slip is dispersed on a high-speed mixer at 18–22 m/s, screened through 100 µm slotted screens, applied with a bent-blade coater, and dried in an infrared/air-cap sequence at 120–160 °C to a sheet moisture of 4–6%. Supercalendering at 40–70 kN/m line load develops gloss and fibre coverage; excessive nip load above 80 kN/m may reduce heat-seal peel strength by causing binder migration and fibre crush. Terminal products include paper cups, folding cartons, frozen food board, and sandwich wrap.
A recurring blade-line defect is whiskering at the trailing edge when coating colour pH exceeds 9.0 from alkaline calcium carbonate addition; pH is therefore maintained at 8.0–8.8, and dispersant demand is checked by zeta potential above -25 mV on a streaming current monitor. Circulation flow through the coating pan is held at 2–3 tank turnovers per hour to prevent sedimentation; flow below 1.5 tank turnovers per hour leads to blade scratches and calender cuts. Medium ethylene VAE grades intended for heat-sealable board are not blended with casein or soy protein above 10 dry parts per 100 parts total binder because protein insolubility can raise viscosity and reduce water resistance after ice-water immersion testing.
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Medium Ethylene VAE Emulsion, designated VAE-ME 55, is a carboxylated vinyl acetate–ethylene copolymer dispersion produced by semicontinuous emulsion polymerization under ethylene pressure. The copolymer contains a copolymerized ethylene mass fraction of 10–20 wt% and is identified by CAS Registry Number 24937-78-8. The dispersion employs a polyvinyl alcohol protective colloid system and is supplied as a milky white liquid with a mild acetic odor. Typical analytical values for a commercial medium ethylene VAE emulsion are shown in the following table. The dispersion is shear-thinning with a flow index of 0.4–0.6 across shear rates from 1 s⁻¹ to 100 s⁻¹ and average particle size by laser diffraction of 0.5–1.5 µm. The product is preservative-free; opened containers require addition of an appropriate biocide. The mildly acidic pH range of 4.0–5.5 prevents premature hydrolysis of the polyvinyl alcohol stabilizer and maintains colloidal charge during storage at 5–35 °C. Freeze–thaw stability is limited to 1–2 cycles unless propylene glycol is added by the formulator.
| Property | Test method | Typical value |
|---|---|---|
| Solids content | ISO 3251:2019 | 54–56 wt% |
| pH | ISO 976:2013 | 4.0–5.5 |
| Brookfield viscosity, 23 °C, spindle 3, 20 rpm | ISO 2555:2018 | 300–800 mPa·s |
| Minimum film-forming temperature | ISO 2115:2018 | 0–5 °C |
| Density | ISO 2811-1:2016 | 1.07–1.09 g/cm³ |
| Residual vinyl acetate monomer | ISO 13741-1:2016 | <0.10 wt% |
Formulation of VAE-ME 55 into woodworking and packaging adhesives is typically carried out in low-shear planetary mixers or anchor agitators operating at 50–150 rpm. The emulsion accepts mineral fillers, plasticizer dispersions, tackifier dispersions, and associative thickeners. pH adjustment with aqueous ammonia or sodium bicarbonate to 6.0–7.0 activates alkali-swellable thickeners and raises Brookfield viscosity from 300–800 mPa·s to 1500–6000 mPa·s depending on thickener solids. In wood adhesion testing according to EN 204:2016, medium ethylene VAE-based adhesives typically meet D2 and D3 durability classes when compounded with 10–20 wt% of a compatible plasticizer or coalescent. Filled formulations can incorporate 30–50 wt% calcium carbonate without loss of adhesive strength if filler particle size is below 20 µm median D50. Viscosity stability during 30-day storage at 23 °C is typically ±10 % of initial value. The processing window is limited by the shear sensitivity of the protective colloid: high-shear dispersers with tip speeds above 15 m/s can generate coagulum and reduce bond strength. Batch temperature should be maintained below 40 °C to avoid thermal destabilization and viscosity drift. Published data for specific equipment configurations is limited beyond these general operating boundaries.
Medium ethylene content alters the glass transition temperature of the copolymer film through internal plasticization. Using the Fox equation, 1/Tg = w(VA)/Tg(VA) + w(E)/Tg(E), with Tg(VA) taken as 28–32 °C and Tg(E) taken as −80 °C, a copolymer containing 15 wt% ethylene exhibits a calculated Tg near −5 °C. This corresponds to a minimum film-forming temperature of 0–5 °C, allowing film coalescence without high-boiling coalescing agents at ambient indoor temperatures. Dynamic mechanical analysis of dried films shows a tan δ peak at −2 °C to 5 °C, confirming internal plasticization without migrating plasticizer. Tensile testing of free films prepared according to ISO 527-3:2018 typically yields tensile strength of 4–8 MPa and elongation at break of 400–700 % for clear films dried 7 d at 23 °C and 50 % RH. The mechanical property cliff-edge occurs at ethylene contents above 20 wt%: tensile strength falls below 3 MPa, while pressure-sensitive tack and elongation rise disproportionately. Below 8 wt% ethylene, films become brittle and crack at 0 °C in mandrel bend tests according to ISO 1519:2021. Peel adhesion on untreated polyethylene is lower than on corona-treated polyethylene; corona treatment to 38–42 dyn/cm surface energy is required for durable bonding. These boundaries define the medium ethylene window for balanced cohesive strength and cold-temperature flexibility.
| Property | Low ethylene (≤10 wt%) | Medium ethylene (10–20 wt%) | High ethylene (> 20 wt%) |
|---|---|---|---|
| Minimum film-forming temperature (°C) | 5–15 | 0–5 | <0 |
| Tensile strength (MPa) per ISO 527-3:2018 | 8–12 | 4–8 | <4 |
| Elongation at break (%) per ISO 527-3:2018 | 100–300 | 400–700 | >700 |
| Water absorption (%) per ISO 62:2008 | 15–25 | 20–40 | 40–60 |
In floor covering, ceramic tile, and wall panel adhesive formulations, medium ethylene VAE emulsion is specified where wet tack on porous substrates, filler acceptance, and low-odor film formation outweigh the ultraviolet resistance of acrylic latex. A direct substitution of acrylic latex with VAE-ME 55 at equal polymer solids typically increases adhesion to polyvinyl chloride and wood by 15–30 % in T-peel testing according to ISO 11339:2022. However, VAE films have higher water sensitivity than all-acrylic films: 24 h water absorption according to ISO 62:2008 is commonly 20–40 wt% for medium ethylene VAE compared with 5–15 wt% for acrylic latex. Therefore, formulation adjustments such as addition of 5–15 wt% of a polymeric water-resistance additive or crosslinker are required for wet-area applications. In production, high-speed dispersers with a Cowles blade at 5–15 m/s tip speed are used to incorporate 30–50 wt% calcium carbonate filler; VAE-ME 55 exhibits lower foam generation than acrylic latex under identical mixing conditions. For carpet lamination, VAE-ME 55 is used with 20–30 wt% filler and 0.5–2 wt% associative thickener to achieve viscosity 5000–15000 mPa·s for troweling or roller application. Published data for specific construction adhesive formulations is limited; the values above are representative of general industrial experience.
When VAE-ME 55 is employed as a binder for nonwoven wipes, carpet backing, or architectural coatings, the emulsion is typically applied by air-knife, slot-die, or roll coating equipment. Mechanical stability under high shear is evaluated in a Waring blender test at 10,000 rpm for 5 min; coagulum content should remain below 0.1 wt% of wet emulsion. In practice, recirculation loops on production coaters can subject the dispersion to cumulative shear at 40–50 °C, which may reduce colloidal stability and increase screen clogging frequency. Diaphragm pumps are preferred over centrifugal pumps to minimize shear-induced grit formation. On a slot-die coater running at 100–300 m/min, the emulsion must maintain foam density below 0.05 g/mL to avoid coating defects. For paint formulations, scrub resistance of VAE-bound flat paints tested per ISO 11998:2006 is generally lower than acrylic-bound equivalents, but wet abrasion resistance improves when 2–5 wt% of a reactive crosslinker such as a polyfunctional aziridine is added before application. Pot life after adding aziridine crosslinker is limited to 4–8 h at 23 °C.
In pressure-sensitive adhesive applications, medium ethylene VAE is blended with tackifier dispersions at ratios between 1:0.5 and 1:1.5 on dry polymer weight. Loop tack on stainless steel per ASTM D6195-03(2019) typically falls in the range 3–8 N/25 mm for medium ethylene grades, lower than high-ethylene VAE but higher than low-ethylene VAE. The emulsion is coated on release liner and dried in a forced-air oven at 80–120 °C for 2–5 min. Because residual water can plasticize the film, equilibrium moisture content after 24 h at 23 °C and 50% RH should be verified before final peeling tests. Published data for this specific configuration is limited; formulators should validate tackifier compatibility with a compatibility panel at 50 °C for 14 d to exclude phase separation.
For textile and nonwoven binder applications, VAE-ME 55 is crosslinked with 0.5–2 wt% of a blocked isocyanate or N-methylol acrylamide derivative to improve solvent resistance. Curing is conducted at 130–150 °C for 1–3 min on a stenter frame. The binder add-on level of 10–20 wt% on fiber weight typically yields dry tensile strength of 100–200 N/50 mm according to ISO 9073-3:2023, but the data for specific fiber types is limited. Because the emulsion is anionically stabilized, it is compatible with nonionic wetting agents but not with cationic softeners.
The polyvinyl alcohol stabilizer in VAE-ME 55 is crosslinked by borate ions. Addition of borax or boric acid at concentrations as low as 0.1 wt% based on wet emulsion raises Brookfield viscosity sharply and can produce irreversible gelation. Multivalent metal salts, including aluminum sulfate and calcium chloride, reduce zeta potential and coagulate the dispersion at concentrations above 0.5 wt%. Cationic surfactants and cationic polymer additives are incompatible and should not be introduced into the emulsion. Solvent addition must be limited to water-compatible glycols and ethers; aromatic and aliphatic solvents above 5 wt% can cause phase separation. pH reduction below 3.0 by acidic additives destabilizes the colloid; pH above 8.0 hydrolyzes acetate groups and releases acetic acid odor. Equipment cleaning after runs with VAE-ME 55 should use warm water at 30–40 °C before the film dries, because dried VAE is not redispersible in cold water.
Regulatory compliance of VAE-ME 55 is supported by residual vinyl acetate monomer below 0.1 wt%, and the product is typically formulated to meet REACH Annex XVII restrictions, RoHS Directive 2011/65/EU for lead, mercury, cadmium, hexavalent chromium, PBB, and PBDE, and relevant sections of FDA 21 CFR 175.105 for indirect food contact adhesives when appropriately formulated. Storage stability from date of manufacture is 6 months at 5–35 °C in sealed original containers. Repeated freeze–thaw cycles are not recommended; if frozen, the emulsion may separate irreversibly and should be discarded. Transport classification according to ADR at ambient conditions is not restricted. The product must not be discharged into surface water without treatment, as it is classified as hazardous to aquatic life according to EC 1272/2008 if not handled properly.