| Código SH | 360052 |
| Nome Do Produto | Emulsão VAE HS-420 de baixa Tg |
| Tipo De Polímero | Emulsão de Copolímero de Acetato de Vinil-Etileno (VAE) |
| Temperatura De Transição Vítrea Tg | Aprox. -15 ° C |
| Conteúdo De Sólidos | 55 ± 1% |
| Viscosidade Brookfield 25 C | 1500 3000 cP |
| O Ph | 4.5 5.5 |
| Temperatura Mínima De Formação De Filme Mfft | Aproximadamente 0°C |
| Tamanho De Partícula | 0,5 2.0 µm |
| Densidade | Aprox. 1,06 g /cm³ |
| Aparência Do Filme | Claro, flexível e pegajoso |
| Monómero Residual De Acetato De Vinilo | <0,1% |
| Estabilidade Congelamento Descongelamento | Estável até 3 ciclos |
| Adesão De Substrato | Bom para substratos de madeira, papel e espuma |
Como uma fábrica acreditada da Emulsão VAE HS-420 de baixa Tg, aplicamos protocolos de qualidade rigorosos - cada lote é submetido a testes rigorosos para garantir padrões de eficácia e segurança consistentes.
| Embalagem | A emulsão HS-420 Low-Tg VAE é embalada em tambores de 200 kg e bolsas IBC de 1000 kg para transporte seguro. |
| Carga de contêiner (20' FCL) | Emulsão VAE HS-420 Low-Tg em FCL 20 ': embalado em tambores /baldes, seguro na vertical, perigo rotulado, recipiente ventilado, sem vazamentos, estável durante o trânsito. |
| Envio | A emulsão HS-420 Low-Tg VAE é enviada em tambores selados, bolsas IBC ou tanques a granel para evitar vazamento e contaminação. Proteja do congelamento, calor extremo e luz solar direta. Armazene entre 5 '35 ° C. Garanta o transporte seguro e vertical com ventilação adequada. Não classificado como mercadoria perigosa de acordo com os regulamentos padrão. |
| Armazenamento | Armazene a emulsão VAE HS-420 Low-Tg em recipientes originais bem fechados em uma área fria, seca e bem ventilada. Mantenha longe da luz solar direta, fontes de calor e materiais incompatíveis. Mantenha a temperatura de armazenamento entre 5 ° C e 35 ° C; não permita o congelamento. Mantenha os recipientes em pé para evitar vazamentos e uso dentro da vida útil recomendada, mexendo antes de usar se ocorrer assentamento. |
| Prazo de validade | Conservar em recipientes selados de origem a 5 graus 35 ° C, protegidos do congelamento. O prazo de validade é de seis meses a partir da data de fabrico. |
Compliance with indirect food additive regulations under FDA 21 CFR 176.170 and 176.180, alongside European Commission Regulation (EU) 10/2011 and its subsequent amendments, governs the formulation of water-based side-seam adhesives for double-wall and single-wall paperboard cups where HS-420 is applied at 95–98 wt% as the principal binder in the adhesive compound. The emulsion, supplied at 55–57% solids with a sub-zero minimum film formation temperature, eliminates the need for fugitive coalescing solvents entirely—a critical design criterion when overall migration limits must remain below 10 mg/dm² of food contact surface. On high-speed cup-forming lines operating at 180–220 cups per minute, such as those built by PMC or Hörauf, the adhesive is transferred via a closed-circuit slot-die coating head or a precision-gravure roll applicator onto the unbleached or clay-coated paperboard shell; the transfer volume is tightly controlled to 3–5 g/m² (wet) to prevent squeeze-out at the seam under the compression station. Downstream, the side-seamed blank passes through a hot-air tunnel where circulating air at 180–220 °C evaporates water and triggers rapid film coalescence. The resultant bond must withstand hot-fill conditions up to 95 °C for coffee and tea without delamination, a requirement verified internally by peel-strength testing per TAPPI T 494 om-22 on specimens conditioned at 23 °C /50% RH and after a simulated hot-liquid hold. A persistent processing conflict emerges from the low glass-transition temperature of HS-420: while the soft polymer backbone grants the seam exceptional cold-impact resistance, it also increases the risk of blocking—that is, adjacent cups adhering to one another within the nested stack under the weight of stacked inventory. Mitigation calls for the incorporation of a small fraction (0.5–1.5 wt% of the formulation) of a high-Tg water-dispersible anti-blocking additive, typically a finely divided polyethylene wax dispersion with a melting point above 130 °C, dispersed homogeneously using a planetary mixer at 100–200 rpm before transfer to the holding tank. Failure to control blocking force below 0.5 N/cm (as measured by the enclosed ASTM D3354-15 method with 48-hour dwell at 40 °C/80% RH) results in cup jamming on automatic de-nesting feeders at the beverage filling plant, a defect that immediately halts production. End articles encompass hot-beverage cups, cold-drink cups with a polyethylene or polylactic acid internal lining, and ice-cream tubs; in each case, the adhesive must maintain seam integrity through condensation cycling without introducing off-odour or off-taste, a sensory attribute validated via organoleptic panel testing according to an adaptation of ISO 13302:2003.
Formulation trials conducted on commercial-scale Cowles-dissolver equipment with a 75 hp motor and a 24-inch high-shear dispersion blade indicate that HS-420 can serve as the dominant binder in white elastomeric roof coatings when the dried film must simultaneously meet the elongation-at-break threshold of ≥400% at -26 °C and a tensile strength of ≥1.4 MPa, both criteria extracted from ASTM D6083-05(2021) Type III liquid-applied roof membrane specifications. The emulsion is typically dosed at 38–48 wt% (wet weight) of the total formulation, replacing styrene-acrylic dispersions that rely on external plasticizers to retain low-temperature flexibility—plasticizers that migrate over time and cause embrittlement of the top surface. During let-down, HS-420 is added after the pigment dispersion phase, which combines titanium dioxide (R-960 grade, 5–8 wt%), calcium carbonate (25–35 wt%), a polysiloxane defoamer (0.2–0.5 wt%), and a low-molecular-weight polyacrylate sodium salt dispersant that has undergone pre-neutralized titration to pH 7.5–8.5. Once the emulsion is incorporated at 500–800 rpm sweep-agitation, the batch must be held within a temperature window of 15–30 °C to avoid shear-induced demulsification; a lift in temperature above 35 °C for more than 20 minutes often triggers micro-coagulum formation that clogs the downstream 60-mesh vibrating screen. Application of the liquid coating onto a sprayed polyurethane foam or concrete deck typically proceeds through an airless spray rig delivering 1.2–1.5 L/min at 180–220 bar tip pressure, followed by a back-roll pass to embed the polyester reinforcement fabric. The low-Tg nature of HS-420 contributes to an inherently inferior dirt-pick-up resistance under accelerated soiling conditions (ASTM D3719-19); therefore, the formulation must be upgraded with a crosslinkable silicone-based surface modifier added at 2–4 wt% post-emulsion. When crosslinked by ambient moisture following application, the modifier functions without diminishing the >500% elongation at -15 °C. The terminal product is a monolithic, vapour-permeable membrane that meets the liquid-water transmission requirement of <0.1 kg/m²·h under EN 1504-2 Class I.
Spunbond bi-component and carded thermally bonded polypropylene nonwovens destined for the absorbent core wrap and backsheet lamination of adult incontinence briefs and feminine hygiene pads require a soft, non-irritating binder whose peel strength does not become the rate-limiting parameter after ultrasonic or thermal-point sealing. HS-420, applied at an add-on rate of 8–15 wt% relative to web basis weight through a spray atomization manifold operating at 0.8–1.5 bar air pressure with a nozzle orifice diameter of 0.4–0.8 mm, penetrates the fibre matrix to form a low-crystallinity film with a measured Martindale abrasion resistance per EDANA/INDA NWSP 120.1.R0 that remains within the 500–900 rubs pass criterion without delamination. The oven profile that follows—typically a through-air drum dryer with a residence time of 4–8 seconds at a peak air temperature of 130–145 °C—drives off water to a residual volatile content below 0.5 wt% while simultaneously activating a minimal degree of interparticle coalescence; full properties develop after 24-hour ambient maturation at >40% RH. Particular attention must be directed to the re-wet characteristic: HS-420 permits a strike-through time of 2.0–3.5 seconds when tested per NWSP 070.1.R0, placing it within the acceptable range for acquisition-distribution layers of high-absorbency products. A processing limitation arises when the manufacturing relative humidity drops below 30%—the evaporative cooling inside the spray chamber can prematurely dry the atomised droplets, leading to a rise in specks and a measurable drop in cross-direction peel strength to below 1.0 N/25 mm (NWSP 120.1.R0), an effect reversible by reintroducing a 2–3 m conditioning plenum immediately upstream of the spray station. Regulatory conformity for skin-contact hygiene articles is established through toxicological risk assessment referencing ISO 10993-1:2018 endpoint evaluations for surface-contact devices with duration exceeding 24 hours, supplemented by a negative result in the OECD 439 in vitro skin irritation assay for the emulsion film extract. Finished consumer goods comprise ultra-thin sanitary napkins, belted absorbent briefs, and underpad sheets; in each construction, HS-420 replaces coarser self-crosslinking acrylics to preserve the drape and quietness of the textile-like backsheet.
Formulation protocols for a water-based polyvinyl acetate-vinyl ethylene laminating adhesive designed for vacuum membrane pressing of matte PVC foil onto moisture-resistant MDF panels centre on HS-420 at 60–75 wt% of the wet blend, co-stabilised with a rosin glycerol ester dispersion (12–18 wt%) to elevate hot-tack and a hydrophobically modified ethoxylated urethane thickener to bring the Brookfield viscosity to 8,000–15,000 mPa·s at 20 rpm spindle 6. The mixture is spray-applied through a gravity-fed pressure pot connected to a 1.2–1.8 mm nozzle, depositing 60–80 g/m² wet onto the pre-sanded MDF core.The process window becomes critically narrow during the heating phase inside a membrane press—typically a Wemhöner or Burkle single-table press equipped with an oil- or water-heated platen and a silicone membrane rated for 0.5–0.7 MPa cavity pressure. Because HS-420 possesses a low glass-transition temperature, full bonding can be achieved at a surface temperature as low as 48–55 °C, considerably lower than the 70–80 °C demanded by conventional vinyl-acetate homopolymers, thereby reducing the risk of PVC gloss change and allowing the use of thinner, temperature-sensitive decorative films. However, this advantage introduces a counter-risk: post-pressing, the adhesive film remains tacky for an extended period (open time >30 minutes at 23 °C) unless the system is catalysed with 0.5–1.0% of a blocked aluminium chloride catalyst that solvates during the heat cycle and accelerates crosslinking with the rosin ester acid groups. Water-resistance classification under EN 204 (D2 and D3 sequences) is satisfied after 24 hours of cold-cure and a further 72 hours of ambient conditioning, with the D3 bond strength exceeding 3.0 N/mm² after soaking in cold water for 4 days and reconditioning. Finished components predominantly serve as three-dimensional kitchen cabinet doors, wardrobe overlay panels, and office furniture fascia, where the adhesive must retain dimensional stability across cyclical humidity swings between 30% and 85% RH without delamination at the foil edge—validated via the heat-resistance test of DIN EN 14257 at 70 °C for 24 hours.
Polymer modification of thin-section structural repair mortars with HS-420 becomes particularly valuable when the substrate demands a bonded overlay with a linear shrinkage below 0.08% and an adhesion pull-off strength above 2.0 MPa, the performance minima set by EN 1504-3 for R4-class repair products. The two-component system combines a pre-packed dry-mix consisting of ordinary Portland cement CEM I 42.5R, graded silica sand (0.1–2.0 mm), powdered superplasticizer (polycarboxylate ether, 0.2–0.6 wt% on cement basis), and a dry defoamer, with a wet admixture where HS-420 is metered at a polymer-cement ratio (p/c) of 0.10–0.15 of emulsion solids per unit mass of binder. Agglomeration and flash-setting are avoided by first blending the dry components with 70% of the total gauging water in a planetary counter-current mixer for 120 seconds, then introducing the HS-420 liquid admixture at low blade speed (140 rpm) over an additional 90 seconds; a separate defoamer dosing typically reaches 0.15–0.25 wt% relative to the emulsion to prevent entrained air volumes above 6%.The specific low-Tg character of HS-420 translates into a modified mortar with a flexural strength exceeding 10 MPa and a static elastic modulus reduced by 30–40% relative to an unmodified reference, permitting active crack-bridging movement in excess of 0.5 mm under the DIN EN 1542 adhesion-with-shear protocol. Nonetheless, an operational boundary must be respected: when the p/c ratio surpasses 0.12 at a constant aggregate-to-binder ratio of 2.5:1, the Vicat initial setting time lengthens from 90 minutes to beyond 180 minutes at 20 °C, and the 28-day compressive strength can decrease by 15–20% because the coalesced polymer film interferes with the hydration product connectivity. This imposes a practical upper dosage limit of approximately 12% polymer solids in load-bearing horizontal patches that must be opened to traffic within 24 hours. Where the application is a vertical levelling mortar for exposed balcony decks, the p/c ratio is reduced to 0.05–0.08 to maintain a pot life above 60 minutes and a sag resistance below 1.0 mm per the empirical rib test. Ultimately, the cured composite forms an impermeable repair screed with a chloride ion migration coefficient below 2.0×10⁻¹² m²/s (NT BUILD 492), functioning as the finished flooring surface and receiving a subsequent polyurethane top-seal coat.
On a contemporary dual-rod making-and-packing cigarette line producing from 8,000 to 10,000 cigarettes per minute, the side-seam adhesive must develop instantaneous mechanical grip within the 5–8 millisecond window before the glued rod enters the furnace section, a constraint that eliminates solvent-based adhesives yet demands an aqueous dispersion stable under extreme shear of up to 3×10⁵ s⁻¹ within the transfer roller nip. HS-420, diluted to a coating-ready viscosity of 800–1,200 mPa·s (Brookfield LVT, spindle 2, 30 rpm) by the controlled addition of deionised water—and occasionally a small quantity of a high-molecular-weight polyvinyl alcohol solution (2–4 wt%) to fine-tune open time—is fed to an engraved chromium-plated transfer roller that deposits a stripe of 1.0–1.5 mm width and 0.02–0.04 mm wet thickness onto the cigarette paper. The immediate dwell under the steamer box initiates a rapid surface-tack development even though the bulk water is not yet evaporated; here, the sub-zero glass-transition temperature of HS-420 allows the polymer to flow and wet the cellulose fibre at ambient factory temperatures as low as 15 °C without the need for a plasticising co-monomer that could later volatilise or migrate into the tobacco column—a persistent problem with dibutyl phthalate-plasticised polyvinyl acetate homopolymers. Conformity to the tobacco industry’s volatile organic compound limitation frameworks, such as the Health Canada T-219 method for formaldehyde and acetaldehyde headspace capture, is facilitated by the ethylene comonomer that internally plasticises the polymer backbone. A documented constraint emerges during summer shifts when chiller failure allows the emulsion in the holding tank to exceed 35 °C: the thermal mobility of the aqueous phase triggers a rise in viscosity drift and can cause the formation of a dehydrated skin on the transfer roller, resulting in erratic glue-line weight and a reject-rate spike beyond 2% at the filter-tipping station. The finished product is a king-size filtered cigarette with a seam burst strength exceeding 1.5 kPa, verified by the enclosed ISO 6565:2015 draw-resistance and integrity test, alongside a sensory verdict of zero flavour interference determined through a trained panel following CORESTA Guide No. 18.
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