| HS Code | 820090 |
| Product Name | Film-forming Resin |
| Chemical Family | Acrylic copolymer |
| Appearance | Transparent viscous liquid |
| Solid Content | 50 ± 2% |
| Viscosity | 2000–5000 mPa·s at 25°C |
| Acid Value | 5–15 mg KOH/g |
| Hydroxyl Value | 40–80 mg KOH/g |
| Glass Transition Temperature | 20–40°C |
| Minimum Film Forming Temperature | 10–20°C |
| Density | 1.02–1.08 g/cm³ at 25°C |
| Flash Point | ≥60°C |
| Voc Content | ≤300 g/L |
As an accredited Film-forming Resin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Film-forming resin supplied in 25 kg sealed fiber drums with inner polyethylene liner, protecting against moisture and contamination. |
| Container Loading (20′ FCL) | Film-forming resin loaded in 20′ FCL: packed in drums or IBCs on pallets, secured, ventilated, moisture-protected to maximize payload. |
| Shipping | Film-forming resins ship in sealed drums or IBCs, protected from moisture and extreme temperatures. Proper labeling, SDS, and compliance with transport regulations are essential. Avoid incompatible materials and ignition sources. Secure upright loading prevents leakage. Ensure ventilation, spill containment, and documentation for safe handling throughout transit. |
| Storage | Store Film-forming Resin in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep containers tightly sealed to prevent moisture contamination or skinning. Maintain temperatures between 5–35°C and avoid extreme temperature fluctuations. Use within manufacturer’s specified shelf life, and ensure proper labeling and segregation from incompatible materials. |
| Shelf Life | Shelf life is typically 12 months when stored sealed in a cool, dry place away from sunlight and moisture. |
Styrene-acrylic film-forming resin with a glass transition temperature of 18 °C and minimum film formation temperature of 12 °C is incorporated at 14.0% binder solids by total formulation weight into a high-PVC interior wall paint. The pigment volume concentration is fixed at 54%, which places the dry film slightly below the critical PVC for the selected TiO₂/extender package; raising PVC above 58% at constant binder solids causes a stepwise loss in ISO 11998:2006 wet-scrub resistance because the binder phase can no longer encapsulate extender particles. Coalescent demand is evaluated by drawdown on a wire-wound bar over a Leneta 2C opacity chart followed by ASTM D3793 low-temperature coalescence at 5 °C. When 2,2,4-trimethyl-1,3-pentanediol monoisobutyrate is dosed below 4.0% on binder solids, visible mudcracking appears in 100 µm wet films cast at 5 °C. Above 6.5% on binder solids, the film remains tack-free after 24 h, but ISO 11998:2006 scrub resistance after 28 days of dark cure drops from Class 2 to Class 3 due to retained plasticizer. Application viscosity is adjusted with an associative polyurethane thickener dosed at 0.3–0.6% of total formulation weight to achieve 1,200–1,500 mPa·s on a Brookfield RVT viscometer spindle 4 at 12 rpm and an ICI cone-and-plate high-shear viscosity of 0.12–0.18 Pa·s at 12,000 s⁻¹. Airless spraying with a 517 tip at 80–100 bar produces a uniform 100 µm wet film after high-speed dispersion at 1,200 rpm for 20 min with a 50 mm cowles blade. Contrast ratio measured by ASTM D2805 reaches 0.95 at 100 µm wet film thickness, and VOC content by ASTM D2369 remains below 30 g/L excluding water and exempt solvents. The terminal interior wall paint conforms to the EU Ecolabel indoor paint criteria.
| Property | Standard / method | Acceptance window |
|---|---|---|
| Low-temperature coalescence | ASTM D3793 | No cracking at 5 °C |
| Wet-scrub resistance | ISO 11998:2006 | Class 2, loss ≤ 20 µm after 28 days |
| Contrast ratio | ASTM D2805 | ≥ 0.95 at 100 µm wet film |
| VOC content | ASTM D2369 | ≤ 30 g/L minus water and exempt compounds |
Raising polyvinyl acetate dispersion solids above 45% in a finished D3 wood adhesive is constrained by colloidal stability rather than final bond strength. A commercial PVAc homopolymer dispersion containing 50% solids and a Brookfield RVT viscosity of 10,000–15,000 mPa·s at 20 rpm is let down to 42%–45% total solids with filler and water; further solids increase without additional protective colloid triggers shear-induced gelation on grooved roller coaters operating at 25–35 m/min. The formulation is built from 70–80 parts PVAc dispersion, 5–10 parts calcium carbonate filler, 2–5 parts plasticizer, and 0.2–0.5 parts associative thickener to maintain a viscosity of 6,000–9,000 mPa·s at 20 °C. Spread rate is controlled at 120–150 g/m² on beech and oak lamellas, with a closed assembly time of 10–20 min and cold-press pressure of 0.7 N/mm² for 20–30 min. Shear strength after 7 days conditioning to EN 205 exceeds 10 N/mm² on beech; water resistance to EN 204 D3 requires no delamination after 4 days of cold-water soak. The operational boundary is relative humidity: at RH above 70%, board moisture content above 12% delays water from the adhesive, and pressing time must be extended by 25% to maintain bond strength. Terminal products include flat-panel edge-glued furniture components and interior joinery.
In water-based pressure-sensitive adhesive constructions, a high-solids acrylic film-forming resin is blended with a rosin-free tackifier dispersion to produce a removable-to-permanent label adhesive. A representative starting ratio is 90 parts acrylic dispersion at 55% solids, 10 parts hydrocarbon tackifier dispersion at 50% solids, and 0.2–0.5 parts high-shear alkali-swellable thickener. The mix is coated onto a 23 µm corona-treated BOPP face stock via reverse-roll or slot-die coating at 20–25 g/m² dry coat weight and dried through a three-zone tunnel with zone temperatures of 60 °C, 80 °C, and 100 °C at line speed 120–180 m/min. Loop tack by ASTM D6195 on stainless steel typically falls between 8 N/25 mm and 12 N/25 mm; 180° peel adhesion by ASTM D3330 after 24 h dwell falls between 6 N/25 mm and 10 N/25 mm. Static shear by ASTM D3654 with 1 kg load at 23 °C remains above 20 h, provided the tackifier level stays below 12 parts. Above that level, low-molecular-weight tackifier migration plasticizes the face stock and produces label adhesive bleed around die-cut edges. The terminal forms are roll-to-roll prime labels and logistics tags.
Nitrocellulose film-forming resin is used in solvent-based gravure inks at 8–12% by weight of the total ink formulation, with a pigment-to-binder ratio ranging from 0.8:1 for high-strength carbon black to 1.5:1 for process yellow. The base solvent blend is ethyl acetate, ethanol, and isopropanol at 60:30:10, and the let-down is adjusted in 5% steps to map a dilution curve. A DIN 53211 cup viscosity of 18–25 s at 23 °C is maintained for rotogravure cylinders engraved at 60–80 lines/cm and running at 180–250 m/min; dilution below 12 s increases misting and produces print mottle on 12 µm polyester film, while viscosity above 27 s fills fine highlight cells and reduces transfer efficiency. Drying tunnel temperatures are kept at 60–75 °C for three zones, with residual solvent in the printed film controlled below 10 mg/m² by headspace gas chromatography. Adhesion to corona-treated PET is tested by ASTM D3359 cross-cut tape removal and must reach class 5B after 24 h; lamination bond strength to aluminium foil is measured by ASTM D1876 T-peel and exceeds 2.0 N/15 mm after solventless laminating adhesive cure. The terminal application is flexo/gravure printed snack food packaging; migration compliance is handled under EU Regulation 10/2011 for the finished laminate and the ink manufacturer’s declaration under the Swiss Ordinance SR 817.023.21 for packaging inks. Nitrocellulose is flame-sensitive, and the process boundary for drying air temperature must remain below 75 °C to avoid adiabatic degradation of retained nitrocellulose fines.
When a hydroalcoholic hair fixative is formulated with a carboxylated acrylate copolymer film-forming resin, the polymer is neutralized with aminomethyl propanol to a pH of 6.5–7.5 before ethanol addition. The resin solids are fixed at 2–6% by weight; below 2% stiffness on hair tresses is insufficient, and above 8% polymer solids produces visible flaking during combing. The hydroalcoholic base is 55:45 ethanol to water for pump sprays, or anhydrous ethanol at 95% with dimethyl ether propellant for aerosol cans. Filtration through a 25 µm cartridge is required to remove gel particles before filling. Spray performance is measured with a Malvern Spraytec laser diffraction system, targeting a Dv90 between 80 µm and 120 µm for a 40 mm actuator. High-humidity curl retention is measured on standard bleached hair tresses at 90% relative humidity and 23 °C for 8 h; a retention above 80% of initial curl is the typical acceptance threshold, though published data for this specific formulation matrix is limited and acceptance windows are established by tress batch lot controls. The terminal finished goods are non-aerosol pump styling sprays and aerosol hairsprays compliant with California CARB VOC limits and EC No 1223/2009 Annex II and III. The primary operational limit is compatibility with alcohol-soluble cationized conditioning agents; combinations with amine-functional silicones can reduce clarity and produce stringy spray patterns.
An aliphatic polyurethane dispersion film-forming resin at 30% solids is let down with water and crosslinked with polycarbodiimide at 2–5 parts per 100 parts dry resin solids to improve hydrolysis resistance and rub fastness on finished automotive leather. The mixture has a pot life of 4–6 h at 25 °C; after that interval viscosity rises beyond 25% of initial value and transfer roller application becomes non-uniform. The topcoat is applied by a closed-cell roller coater at 40–60 g/m² wet coat weight on finished leather, dried in a tunnel at 80 °C for 2 min, and embossed at 120 °C and 80 bar compression. Flex endurance is tested on an ISO 5402 flexometer; at 4 parts crosslinker the coating withstands more than 50,000 cycles without visible cracking, while raising crosslinker to 6 parts reduces flex resistance to under 12,000 cycles because the network becomes too dense. Fogging on DIN 75201 remains below 2.0 mg at 4 parts crosslinker; increase to 6 parts raises fogging values due to residual unreacted crosslinker. Adhesion measured by ISO 2409 cross-cut remains at class 0 at the standard film thickness. The terminal application is pigmented and clear topcoats for automotive seating; compliance includes flammability testing to FMVSS 302, VOC limits in the manufacturing facility, and REACH Annex XVII restrictions for leather chemicals. The process boundary is ambient humidity: above 70% relative humidity, the water-borne topcoat dries slowly and the crosslinker may be consumed by humidity before film formation completes, reducing final rub fastness.
| Compliance property | Standard / method | Acceptance window |
|---|---|---|
| Flex fatigue | ISO 5402 | > 50,000 cycles at 4 parts crosslinker |
| Fogging | DIN 75201 | < 2.0 mg |
| Cross-cut adhesion | ISO 2409 | class 0 |
| Flammability | FMVSS 302 | pass |
For pigment printing on woven cotton and cotton-rich blends, a self-crosslinking acrylic film-forming resin is dosed at 12–18% of the total aqueous print paste. The paste also contains 3–8% pigment dispersion, 1.5–2.5% synthetic thickener, and 1% blocked-isocyanate fixer where higher wash fastness is required. Flatbed screen printing uses polyester mesh counts from 43 to 80 threads/cm; the print paste viscosity is adjusted to 20,000–35,000 mPa·s on a Brookfield RVT spindle 6 at 20 rpm to eliminate sawtooth edge defects. After printing, the fabric is dried at 120 °C for 1 min and cured at 150 °C for 3 min in a hot-air loop dryer. Dry crock fastness tested by ISO 105-X12 reaches grade 4, wet crock reaches grade 3–4, and wash fastness tested by ISO 105-C06 at 40 °C achieves grade 4 on cotton. Binder content above 20% produces a stiff handle and poor drape, while binder content below 10% reduces crock fastness below grade 3 on dark shades. The terminal products are screen-printed apparel, home textiles, and upholstery panels that meet Oeko-Tex Standard 100 requirements for formaldehyde and APEO residues. The operational boundary is fabric absorbency: on untreated hydrophobic polyester, wetting must be pre-adjusted with a nonionic wetting agent or the acrylic film will not penetrate the yarn structure and crock fastness will drop by at least one grade.
Competitive Film-forming Resin prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: admin@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Film-forming Resin FFR-2400 is an anionically stabilized aqueous acrylic copolymer dispersion supplied at 42–46% non-volatile content by mass. The product is used as a primary binder where ambient-cure film integrity, low minimum film formation temperature, and resistance to hydrophilic plasticizer migration are required in a single-component system. Unlike high-glass-transition hard resins that require substantial coalescent loading, FFR-2400 undergoes particle deformation and interdiffusion at substrate temperatures above 5°C, producing a continuous film without the addition of volatile organic coalescents under normal drying conditions. The dispersion is preserved with a formaldehyde-free biocide system and is manufactured under a documented batch-release protocol that includes residual monomer control by ISO 13741-1.
| Property | Method | Acceptance range | Unit |
|---|---|---|---|
| Non-volatile content | ISO 3251:2019 | 42–46 | % by mass |
| pH at 25°C | ISO 976 | 7.5–8.5 | — |
| Brookfield viscosity | ISO 2555 | 200–800 | mPa·s |
| Minimum film formation temperature | ISO 2115 | ≤5 | °C |
| Glass transition temperature, midpoint | ISO 11357-2 | 8–12 | °C |
| Density at 20°C | ISO 2811-1 | 1.02–1.04 | g/cm³ |
| Residual monomers | ISO 13741-1 | ≤500 | mg/kg |
Lot release is governed by the ranges shown above. Viscosity is measured at 25°C using a Brookfield LV spindle 2 at 30 rpm; values outside the window indicate shear-induced coagulation or bacteriological degradation. The shear-thinning index calculated from Brookfield viscosity at 2 rpm and 20 rpm is typically 1.2–1.6; values above 2.0 suggest partial flocculation or polymer gel formation. Batch-to-batch variation in non-volatile content greater than ±1 percentage point has been observed to shift dry film thickness on roll-coating lines by more than 8% at constant wet film application.
During high-shear mixing with a rotor-stator device at 10 000 min⁻¹, the dispersion shows viscosity reduction of 15–25% within 5 minutes and recovers to 90% of initial value within 24 h. Permanent viscosity loss of more than 30% indicates coagulum formation, which is quantified by filtration through a 100 µm sieve per ISO 4576. This behavior constrains the dispersion of pigments and extenders: the resin is not added to the high-shear grind but is used as a letdown binder after the millbase reaches a Hegman grind of 7 or finer per ISO 1524.
Formulating with FFR-2400 in architectural semi-gloss topcoats at 18–22% pigment volume concentration generally yields wet-scrub resistance above 1000 cycles when tested in accordance with ASTM D2486 after 28 days of cure at 23°C and 50% relative humidity. The dispersion is added to the letdown stage after pigment grinding; high-shear dispersion of the resin itself is avoided because prolonged Cowles blade exposure at tip speeds above 15 m/s introduces microfoam and can reduce filter throughput on 250 µm bag filters. Open time measured by ASTM D7488 is extended by 3–5 minutes compared with hard styrene-acrylic controls at the same solids, but this benefit is lost if the wet film is exposed to air velocities above 2 m/s before coalescence is complete. Below 50% relative humidity, wet edge falls below 4 minutes, requiring the addition of 5–10% propylene glycol or a slow-evaporating glycol ether; overdosing propylene glycol above 12% on total formula delays through-dry beyond 24 h and depresses block resistance.
Hard acrylic polyols and styrene-acrylic dispersions with glass transition temperatures above 40°C exhibit minimum film formation temperatures that approach their Tg. Such binders require 8–12% coalescent on binder solids to depress MFFT below ambient, increasing volatile organic compound content under Directive 2004/42/EC Annex II calculations. FFR-2400 reduces coalescent demand to 0–2% because its DSC midpoint Tg is 8–12°C and its particle shell contains lower molecular weight oligomer that plasticizes interfacial diffusion. This difference is measured by ISO 17895 VOC content and by ASTM D6886 gas chromatographic speciation of coalescents. Films formed from hard resins without adequate coalescent typically show mudcracking below 10°C and tensile strength loss after water immersion due to residual hydrophilic coalescent; FFR-2400 films retain adhesion on chalky alkyd substrates under ASTM D3359 tape pull.
Film formation proceeds through three stages: water evaporation and particle ordering, particle deformation driven by capillary pressure and polymer-air interfacial tension, and interdiffusion of polymer chains across particle boundaries. For FFR-2400 at 23°C and 50% relative humidity, the open time before irreversible particle packing is approximately 8–12 minutes. The particle deformation stage is complete only when the wet film temperature exceeds the minimum film formation temperature; below that threshold, residual particle boundaries scatter light and reduce gloss at 60° measurement geometry by 20–30 units compared with fully coalesced films. This behavior is evaluated by ISO 2813 specular gloss and by ASTM D523.
| Parameter | FFR-2400 | High-Tg styrene-acrylic dispersion | Alkali-soluble acrylic support resin |
|---|---|---|---|
| Film formation mechanism | Particle coalescence below 5°C | Coalescent-plasticized coalescence above 40°C | Solution-to-gel transition after amine evaporation |
| Glass transition temperature, ISO 11357-2 | 8–12°C | 45–60°C | 30–40°C acid form |
| Minimum film formation temperature, ISO 2115 | ≤5°C | 40–50°C without coalescent | Not applicable as sole binder |
| Coalescent demand on binder solids | 0–2% | 8–12% | 0% neutralized |
| Tensile elongation at break, ASTM D638, 0.5 mm dry film | 250–350% | 5–10% | <3% |
| Water sensitivity after 24 h immersion, ASTM D870 | None to slight haze | Moderate haze with coalescent leaching | High; resolubilizes |
Compared with long-oil alkyd emulsion, FFR-2400 develops early water resistance more rapidly because film formation does not depend on oxidative crosslinking. However, ultimate solvent resistance and gloss retention under accelerated weathering are lower; unpigmented FFR films exposed in QUV-A per ISO 16474-3 typically show 20–30% gloss loss after 500 h, whereas alkyd systems may retain higher gloss due to crosslink density. This trade-off constrains exterior high-gloss applications but is less relevant in interior and industrial primers where early block resistance and low odor are required.
On a 450 mm pilot reverse-gravure coater running silicone-coated release liner at 120 m/min, FFR-2400 was applied at 20 g/m² dry coat weight and dried in a three-zone oven with web temperatures of 60°C, 90°C, and 110°C. Loop tack measured by ASTM D6195 on stainless steel remained above 12 N/25 mm after 24 h dwell. Published data for this specific configuration is limited; the values reflect a single pilot trial and are not a specification. The dispersion accepts rosin ester tackifier dispersions up to 15 wt% on binder solids without macroscopic coagulation, but addition beyond this level increases shear adhesion failure temperature and reduces removability from painted surfaces.
On blast-cleaned steel with Sa 2.5 surface preparation per ISO 8501-1, FFR-2400 can be formulated into waterborne direct-to-metal coatings at 150–200 µm wet film thickness. Flash rusting is controlled by incorporating an organic corrosion inhibitor at 0.5–1.0% on total formula; without this addition, early rust bleeding appears within 4 h at 80% relative humidity. Salt spray resistance after 240 h per ISO 9227 is highly dependent on substrate profile and edge coverage; published data for this specific configuration is limited. Sag resistance at 150 µm wet film per ASTM D4400 is 18–24 mils after addition of 0.2–0.5% associative thickener.
When substrate temperature is below 10°C, the drying rate must be managed so that the wet film remains above its minimum film formation temperature during particle coalescence. Airless spray application at 180–210 bar with a 0.015–0.019 in tip produces a wet film thickness of 80–120 µm; at 5°C and 65% relative humidity, water evaporation can lower the film surface temperature by 2–4°C, pushing it below the MFFT. The resulting defect is microcrazing rather than cohesive failure. Preconditioning the substrate to 12°C or adding 1–2% dipropylene glycol n-butyl ether on binder solids is required for exterior application below 7°C. Dry-through is evaluated by ISO 9117-3; failure before 4 h at 10°C indicates coalescent deficiency or over-thinning.
For water-based flexographic inks on corona-treated BOPP at 38–42 mN/m surface energy, FFR-2400 is combined with a styrene-acrylic pigment grind base rather than used as the sole grinding vehicle. The film-forming resin provides resolubility control because its acid number is 18–22 mg KOH/g, allowing press-side cleanup with dilute ammonia while resisting water pickup after the ink has dried. Print samples tested by ASTM D5264 Sutherland rub show acceptable scuff resistance after 24 h ageing; immediate blocking on rewind at 40°C is controlled by adding 1–2 wt% high-density polyethylene wax dispersion.
Direct food-contact use is excluded unless the finished article is evaluated under FDA 21 CFR 175.300 or EU Framework Regulation (EC) No 1935/2004 for the specific end use. The dispersion is anionically stabilized; addition of polyvalent cations such as Zn²⁺ above 0.1% on binder solids can cause grit formation. Avoid combination with amine-based additives that remain in the dry film above 0.5% because retained amines increase water sensitivity and delay block resistance development. Formaldehyde-free preservation limits resistance to repeated bacterial challenge; once opened, material should be consumed within 6 months or re-tested by ISO 11930 challenge testing before use.