| HS Code | 559455 |
| Product Name | Butvar B-74 |
| Chemical Family | Polyvinyl butyral (PVB) |
| Physical Form | White granular powder |
| Specific Gravity | 1.083 - 1.090 at 20°C |
| Glass Transition Temperature | 65 - 70°C |
| Molecular Weight Mw | Approximately 120,000 |
| Hydroxyl Content | 17.5 - 20.0 % as polyvinyl alcohol |
| Acetate Content | 0 - 2.5 % as polyvinyl acetate |
| Butyral Content | Approximately 80 % as polyvinyl butyral |
| Viscosity | 2,000 - 4,000 mPa·s at 20°C (15 wt% solution in methanol) |
| Softening Point | 120 - 130°C |
| Tensile Strength | Approximately 28 MPa (film) |
| Elongation At Break | Approximately 180 % (film) |
| Refractive Index | 1.48 - 1.49 |
As an accredited Butvar B-74 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Butvar B-74 polyvinyl butyral resin is supplied as a free-flowing white powder in 25 kg multiwall paper bags. |
| Container Loading (20′ FCL) | Butvar B-74 loaded in 20′ FCL: palletized 25 kg bags, securely braced, moisture-protective lining, ventilation maintained. |
| Shipping | Butvar B-74 ships as a non-hazardous polyvinyl butyral resin in sealed multi-layer bags or fiber drums, palletized and wrapped. Use dry, ventilated containers to avoid moisture uptake. Minimize dust, keep away from heat/sparks, and protect from damage. No special transport classification or UN number required. |
| Storage | Store Butvar B-74 in a cool, dry, well-ventilated area away from heat, open flames, and ignition sources. Keep the container tightly sealed to prevent moisture absorption and contamination. Avoid storage near strong oxidizers. Maintain temperatures between 10–30°C, protect from direct sunlight, and use within the manufacturer’s recommended shelf life. |
| Shelf Life | Butvar B-74 has a shelf life of at least two years when stored in original containers under cool, dry conditions. |
In coil and airframe pretreatment lines where solvent-borne two-pack wash primers are specified for adhesion to mill-finish 3003/5052 aluminum, hot-dip galvanized steel, and zinc electroplate, Butvar B-74 functions as the acid-compatible binder phase that remains film-forming at pH 2.0–4.0 after addition of phosphoric acid. The polyvinyl butyral backbone supplies hydroxyl content of 17.5–20.0% as polyvinyl alcohol equivalent and glass transition temperature of 72–78°C, which allows the cured primer to resist binder re-flow when a polyester or epoxy polyamide topcoat is applied after flash-off. This type of etch primer is not a universal repair coating; it is an adhesion-promoting pre-treatment that is applied to a dry film thickness of 5–8 μm and must be topcoated within the pot-life window of the mixed acid component.
Surface preparation follows ISO 8501-1:2007 cleanliness evaluation; for existing galvanized surfaces the alkaline cleaner must leave a water-break-free surface, and the rinse water conductivity should remain below 50 μS/cm to prevent zinc salt residues that cause white rust under the wash primer. The specified application window is 10–35°C at relative humidity below 85%; spraying below 10°C retards acid reaction with zinc and produces uneven adhesion. Formulation addition is typically 4–8 wt% Butvar B-74 on total two-pack mix. In a 100 kg Part A batch, this corresponds to 12–24 kg of Butvar B-74 solution at 25 wt% solids, 45–60 kg of solvent blend comprising isopropanol, methyl ethyl ketone, n-butanol, and toluene with water content held below 0.5 wt%, 20–35 kg of non-chromate anti-corrosive pigment such as aluminum triphosphate, zinc molybdate, or silica-modified calcium phosphate, and 0.2–1.0 kg wetting/anti-settling additive. Part B is added just before application; Part B contains 85% phosphoric acid diluted to 10–20 wt% active acid in isopropanol/water at a mix ratio of 1:1 to 1:2 Part A/Part B by volume.
Processing equipment on a contract coating line consists of a stainless steel double-walled vessel with a Cowles dissolver at 800–1200 rpm; jacket temperature is set at 25°C because addition of phosphoric acid to a Butvar B-74 solution generates exothermic hydrolysis of residual ester groups and can produce a 4–8% viscosity rise within 30 min. The mixed primer is filtered through a 80–100 mesh bag before air-assisted airless spray at 2.0–2.5 bar atomization pressure, using a fluid nozzle of 0.28–0.38 mm to achieve wet film 10–15 μm. On a continuous coil line, roll coating may be substituted with reverse roll speed ratio 1.2–1.5 and line speed 15–30 m/min. End-article categories include extruded architectural aluminum curtain-wall components where the wash primer replaces hexavalent chromium conversion coatings on exposed edges, galvanized steel storage tank shells that require rapid primer curing before polyurethane topcoating, and aircraft structural ribs where the etch primer is specified by maintenance manuals to restore adhesion after mechanical stripping. System test acceptance is normally verified under ISO 9227:2017 neutral salt spray for 500–1000 h depending on corrosivity class C3 or C4 per ISO 12944-5:2019, with scribe creep below 2.0 mm and cross-cut adhesion classification 0–1 per ISO 2409:2013. Operational limits are sharp: addition of Butvar B-74 above 8 wt% in the two-pack mix increases low-shear viscosity beyond 45 s ISO 2431:2019 cup 4 and reduces pot life to under 4 h at 25°C due to acid-catalyzed chain scission. Chromate pigments, although historically used at 20–35 wt% of non-volatile, are not included in new formulations because hexavalent chromium is subject to REACH authorisation requirements; published data for exact substitution ratios in aerospace-qualified wash primers is limited and must be validated per airframe OEM process specifications.
| Control parameter | Requirement | Standard/equipment |
|---|---|---|
| Dry film thickness | 5–8 μm | ISO 2808:2019 |
| Cross-cut adhesion | 0–1 | ISO 2409:2013 |
| Neutral salt spray scribe creep after 500 h | < 2.0 mm | ISO 9227:2017, ISO 12944-5:2019 |
| Solvent water content | < 0.5 wt% | Karl Fischer titration |
| Mixed primer pot life | 4–8 h at 25°C | ISO 2431:2019 cup 4 |
Flexographic and rotogravure inks that print on corona-treated low-density polyethylene, biaxially oriented polypropylene, and cast polypropylene at line speeds above 150 m/min require a co-binder that does not redissolve the primer layer during high-temperature extrusion lamination. Butvar B-74 is added at 2–6 wt% of the total liquid ink, equivalent to 10–20% of total binder non-volatile, in systems where nitrocellulose or polyurethane alone exhibits inadequate adhesion after exposure to molten LDPE at 300–325°C nip temperatures. The PVB resin contributes hydroxyl groups that bond to carboxylic acid and carbonyl groups created on film surfaces by corona discharge at 38–42 mN/m surface tension per ASTM D2578-17.
Food-contact compliance is established under FDA 21 CFR 175.300 for resinous and polymeric coatings and EU Regulation (EU) No 10/2011 Annex II overall migration limit 10 mg/dm². For dry-food packaging, the finished printed film must also meet Swiss Ordinance SR 817.023.21 for printing inks, particularly when the print is buried rather than surface-printed. Typical ink formula includes 30–35 wt% solvent blend of ethyl acetate, n-propanol, and polyglycol ether acetate, 15–20 wt% nitrocellulose, 2–6 wt% Butvar B-74, 15–20 wt% polyurethane, 10–15 wt% plasticizer of citrate or adipate type, 10–20 wt% pigment, and 1–2 wt% wax/defoamer. The Butvar B-74 solution should be pre-diluted to 20–25 wt% solids before addition to the letdown, because direct addition into an ester-rich letdown can create localized viscosity spikes that overload the recirculating pump.
Processing is performed on a central-impression flexographic press with 8 or 10 color decks, doctor chamber pressure 0.2–0.4 bar, anilox rolls of 200–400 lines per inch and cell volume 4–8 cm³/m², and web tension maintained at 60–120 N/m for 20–40 μm PE film. Drying is by high-velocity hot-air hoods at 40–60°C; residual solvent must be below 5 mg/m² per internal laminator specification because retained solvent causes tunnel defects during extrusion coating. Rotogravure inks based on Butvar B-74 are reduced to printing viscosity 18–25 s ISO 2431:2019 cup 3 before filling the enclosed doctor chamber. Finished article classes include high-gloss confectionery wraps printed on metallized OPP, frozen-food polyethylene duplex pouches, and stand-up barrier laminates where the ink remains buried between PE film and molten extrudate. In retort processes, Butvar B-74 is not recommended because saturated steam at 121°C can progressively hydrolyze the acetal rings and reduce lamination bond strength; published data for this specific configuration is limited.
When co-fired alumina and LTCC glass-ceramic tapes are cast from high-solids slurries requiring binder systems that depolymerize cleanly below 400°C without residual soot, Butvar B-74 is selected over lower-molecular-weight PVB grades because its longer chain length contributes green strength at lower binder fractions. Compliance constraints derive from the sintered component route rather than the polymer itself: lead-free LTCC dielectrics must satisfy Directive 2011/65/EU RoHS Annex II restrictions on lead, and binder burn-out is validated by thermogravimetric analysis under ASTM E1131-20 in air at a heating ramp of 0.5–2.0°C/min. Green sheet thickness is measured by contact profilometry as ±5 μm across a 30 cm-wide tape, and sintered substrate camber is controlled below 0.5 mm/100 mm per internal co-firing specification.
Slurry formulation uses 6–12 wt% Butvar B-74 on dry ceramic mass, 3–6 wt% plasticizer of benzyl butyl phthalate or diethyl adipate type on dry ceramic mass, 0.5–1.5 wt% dispersant, 45–55 wt% ceramic powder or glass-ceramic powder, and 35–45 wt% solvent blend of methyl ethyl ketone and ethanol in a ratio of 40:60 to 60:40. The Butvar B-74 content is deliberately kept below 12 wt% because cast tapes with higher binder levels tend to exhibit green density gradients that produce edge-lift during lamination. Milling is carried out in polyethylene jars with yttria-stabilized zirconia balls of 5 mm diameter at a media-to-slurry volume ratio of 1.5:1 for 16–24 h. After milling, the slurry is vacuum de-aerated at 80–100 mbar for 20–40 min to remove dissolved air and slow solvent evaporation.
Tape casting proceeds on a doctor-blade coater with blade gap 150–500 μm and carrier speed 0.5–1.5 m/min; drying is split into a first zone at 25–40°C and a second zone at 60–80°C to avoid skinning because Butvar B-74 forms a surface film rapidly from methyl ethyl ketone-free solutions. Lamination of printed green sheets at 60–80°C under 20–30 MPa for 30–120 s produces unfired multilayer blocks that are then diced or punched before binder burn-out. Burn-out uses a controlled ramp of 0.5°C/min to 250°C with a 1–2 h hold, followed by 0.5°C/min to 450–500°C; residual carbon must remain below 0.05 wt% of sintered mass. Final components include base-metal-electrode multilayer ceramic capacitors with 2–10 μm dielectric layers, LTCC radio-frequency modules for automotive radar, and co-fired alumina packages for pressure sensors. The hydroxyl-rich Butvar B-74 grade is moisture-adsorbing; green tape stored above 60% RH for more than 24 h can exhibit lamination slippage and should be re-dried at 50°C for 2 h before via punching.
Wood finishing lines that use nitrocellulose lacquers on open-pore mahogany or MDF edge profiles add Butvar B-74 at 5–10 wt% of non-volatile binder to reduce cold-checking and improve intercoat adhesion. The sealer is built on nitrocellulose 15–20 wt%, Butvar B-74 solution 5–10 wt%, short-oil alkyd 5–8 wt%, dibutyl phthalate 2–4 wt%, and an ester/ketone/glycol ether solvent blend to total solids 22–28 wt%. Compliance for coated children's furniture and toys requires migration testing under EN 71-3:2019 and, where used as a barrier sealer on composite wood, the final article may fall under CARB ATCM 93120 for formaldehyde emissions from the substrate rather than the coating.
High-shear dispersion is performed in a stainless steel mixing vessel at 800–1000 rpm until fineness of grind reaches Hegman 5–6, equivalent to 25–40 μm, measured by ASTM D1210-05. Spraying uses HVLP guns at 0.8–1.2 bar atomization pressure, fluid viscosity 30–40 s ISO 2431:2019 cup 4, and wet film 25–35 μm per coat. Between-coat sanding uses 320–400 grit stearated paper; Butvar B-74 reduces clogging relative to high-aliphatic nitrocellulose-only coats because it embrittles less under local sanding heat. Representative finished articles are office desktops with UV-cured topcoats, lacquered kitchen cabinet doors, and children's stamped wooden toys that require a clear sealer below pigmented nitrocellulose topcoat. Above 12 wt% Butvar B-74 on non-volatile, the sealer becomes too elastic and resists dry sanding; below 5 wt%, adhesion to MDF edge banding after 48 h water immersion shows measurable edge whitening.
For aluminium foil lidding stock of 20–30 μm thickness that is heat-sealed to PVC, PET, or PS trays, a gravure-applied lacquer must provide hydrogen-bonding adhesion to aluminium oxide and controlled cohesive failure at peel. Butvar B-74 is combined with vinyl or acrylic heat-seal resins at 8–15 wt% of wet lacquer, while heat-seal resin occupies 10–20 wt%, plasticizer 2–5 wt%, antiblocking wax 0.5–2 wt%, and solvent blend of methyl ethyl ketone, ethyl acetate, and cyclohexanone to total solids 15–25 wt%. Food-contact status is controlled under FDA 21 CFR 175.300 for resinous and polymeric coatings and EU Regulation (EU) No 10/2011 Annex II overall migration limit of 10 mg/dm²; pharmaceutical blister lidding is additionally assessed for packaging extractables under relevant pharmacopeial packaging suitability criteria.
Application is by two-roll gravure coating at 120–200 m/min on foil temper H18; lacquer coat weight is 2–4 g/m² dry; oven zones are set at 80°C, 110°C, and 150°C; residence time is 4–8 s. Heat-seal conditions on high-speed lidding machines use tool temperature 140–180°C, pressure 0.3–0.5 N/mm², and dwell 0.3–0.8 s; seal strength measured as 8–15 N/15 mm peel under ASTM F88/F88M-21. End-use categories include dairy yogurt lidding, beverage portion cups, and pharmaceutical blister lidding. Not suitable for retort lidding above 121°C because seal strength decays under saturated steam hydrolysis; published data for this specific configuration is limited.
In flexible packaging dry-bond lamination, two-component polyurethane adhesives used on PET-to-aluminium and metallized CPP structures show measurable bond strength improvement when Butvar B-74 is pre-dissolved at 20 wt% solids in ethyl acetate and added to the polyol component at 4–8 wt% of final adhesive solids. The Butvar B-74 is added before isocyanate crosslinker introduction to avoid hydroxyl competition and local gel particles; the curing agent index is maintained at NCO/OH 1.2–1.6 to compensate for the additional hydroxyl groups contributed by the PVB. Compliance for food-contact laminates is established under FDA 21 CFR 175.105 and EU Regulation (EU) No 10/2011 Annex II overall migration limit 10 mg/dm²; bond durability is evaluated by T-peel testing under ISO 11339:2010.
Application is performed on a dry-bond laminator with heated gravure smoothing roll at 45–65°C using a roller with 100–140 lines per cm cell count, coating weight 1.8–2.8 g/m² dry, and three-zone air flotation dryers at 60°C, 75°C, and 85°C. Nip lamination runs at 60–80°C and 3–5 bar pressure; the laminated reel is conditioned at 35–45°C for 24–48 h before slitting. Finished structures include dry snack stand-up pouches, metallized confectionery film, and aluminium-laminated lidding for low-moisture pharmaceutical powders. Because PVB is moisture-permeable and can hold residual ester solvent, the system is not recommended for retort pouches or boiling-water sterilisation; published data for those conditions is limited.
Competitive Butvar B-74 prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Butvar B-74 is a polyvinyl butyral resin supplied by Eastman Chemical Company as a free-flowing white powder with a specific gravity of 1.10 (ISO 1183-1). The polymer is synthesized through acid-catalyzed acetalization of polyvinyl alcohol with butyraldehyde; residual hydroxyl content is controlled in the 18–20 wt% range calculated as polyvinyl alcohol, corresponding to a hydroxyl equivalent weight between 240 and 250 g/eq. The weight-average molecular weight typically falls between 120,000 and 150,000 g/mol, and a 10 wt% solution in 60:40 toluene:ethanol at 25 °C develops a Brookfield viscosity of 300–600 mPa·s. Differential scanning calorimetry places the glass transition temperature at approximately 63 °C. These characteristics place the grade between the lower-viscosity Butvar B-76 and the higher-viscosity Butvar B-72. The residual hydroxyl functionality permits covalent integration with phenolic, melamine-formaldehyde, and isocyanate crosslinkers, while the linear acetal structure contributes to film toughness and substrate wetting. Primary industrial applications include solvent-borne structural adhesives, corrosion-resistant metal primers, ceramic greenware binders, and high-cohesion flexible packaging coatings.
The differentiation within the Butvar product line is primarily molecular weight and solution rheology. Butvar B-79, with a weight-average molecular weight near 50,000–80,000 g/mol and a 10 wt% solution viscosity of 25–45 mPa·s, can be formulated at high solids and low solvent demand but exhibits measurably lower cohesive strength and higher cold flow. Butvar B-76, at 90,000–120,000 g/mol, improves film cohesion. Butvar B-74 further increases both molecular weight and solution viscosity to 300–600 mPa·s, which raises lap shear strength and creep resistance without reaching the processing viscosity of Butvar B-72 at 800–1,200 mPa·s. In practical terms, Butvar B-74 requires approximately 25–35% more solvent than Butvar B-76 to reach an equivalent spray viscosity of 100 mPa·s, but the dried film retains greater chain entanglement and improved resistance to slow deformation at 80 °C. Published manufacturer data for this specific configuration is limited to comparative rheology rather than absolute batch specifications.
| Property | Butvar B-79 | Butvar B-76 | Butvar B-74 | Butvar B-72 |
|---|---|---|---|---|
| Weight-average molecular weight (g/mol) | 50,000–80,000 | 90,000–120,000 | 120,000–150,000 | 170,000–250,000 |
| Viscosity, 10 wt% in 60:40 toluene:ethanol at 25 °C (mPa·s) | 25–45 | 80–150 | 300–600 | 800–1,200 |
| Glass transition temperature (°C) | 62 | 62 | 63 | 63 |
| Hydroxyl content, calculated as polyvinyl alcohol (wt%) | 18–20 | 18–20 | 18–20 | 18–20 |
Values in the table are representative manufacturer data for relative grade positioning; specification limits are agreed per batch.
On a production-scale mixer equipped with a Cowles disperser, Butvar B-74 is typically added to the vortex of a solvent blend containing 60–70 mass % toluene and 30–40 mass % ethanol, or an 85:15 methyl ethyl ketone:ethyl acetate mixture. The disperser tip speed is maintained between 10 and 15 m/s for initial wet-out; the batch temperature is held below 40 °C to limit solvent loss and prevent partial solvation that produces gel aggregates. At 20 °C and 15 wt% solids, complete dissolution commonly requires 45–90 min. When ambient relative humidity exceeds 60%, pre-drying at 40–50 °C for 2–4 h is necessary because residual moisture competes for hydrogen-bonding sites and increases solution haze. Final filtration through a 25–50 μm bag is recommended before coating or adhesive compounding. Viscosity drift after 24 h is generally below ±5% when the vessel is sealed and solvent composition is controlled.
Addition of 15–30 wt% Butvar B-74 on resin solids to a phenolic resole or melamine-formaldehyde coating increases tensile strength and reduces brittleness as measured by ASTM D638-14. The hydroxyl equivalent weight of 240–250 g/eq requires 0.40–0.45 equivalents of isocyanate or methylol functionality per 100 g of resin for stoichiometric chain extension. In a two-component epoxy structural adhesive, Butvar B-74 is pre-dissolved at 10–12 wt% in methyl ethyl ketone and introduced into the epoxy component before combination with a polyamide hardener. Lap shear specimens prepared from degreased 2024-T3 aluminum and tested at 23 °C and 50% RH according to ASTM D1002-19 commonly fall in the 15–22 MPa range after 7 days of cure. Published data for longer humid aging of this exact formulation configuration is limited beyond 1,000 h. Gel time decreases nonlinearly when crosslinker concentration exceeds 0.50 equivalents per equivalent of hydroxyl, and the formulation must be processed within 4–6 h at 30 °C to avoid a viscosity increase above 100% of initial value.
In oxide and non-oxide ceramic tape casting, Butvar B-74 serves as a thermoplastic binder because the residual hydroxyl groups interact with particle surfaces and the high molecular weight reduces particle settling. A typical alumina or aluminum nitride slurry contains 35–45 vol% ceramic powder, 3–6 vol% Butvar B-74, and a 50:50 toluene:ethanol solvent system; the slurry is degassed until viscosity falls below 500 mPa·s to remove entrapped air before casting. The high molecular weight of Butvar B-74 increases green tape tensile strength and improves dimensional tolerance during punching and lamination. During burnout, the resin decomposes in air between 250 and 450 °C, and the low ash contribution after 600 °C burnout is generally below 0.1 wt% of the original binder mass. Batch-to-batch variation in binder solution viscosity can alter cast tape thickness by 3–8% if the slurry is not adjusted by solvent addition or cast gap.
Butvar B-74 is soluble in alcohols, glycol ethers, ketones, and chlorinated solvents, but insoluble in water, aliphatic hydrocarbons, and most plasticizer oils. The acetal linkages are susceptible to acid-catalyzed hydrolysis below pH 3; therefore long-term exposure to phosphoric acid etch primers should be evaluated by adhesion retention testing rather than assumed. Waterborne formulations without co-solvent should be avoided because the resin will form unstable dispersions or precipitate. Storage below 30 °C and 50% RH in sealed containers minimizes moisture uptake and free-flow retention. The polymer is exempt from registration under REACH Title II, Article 2(9) as a polymer; monomers and auxiliary substances must still meet registration requirements. Food-contact use may fall under FDA 21 CFR 175.300 for final resinous and polymeric coatings, but extraction testing is formulation-specific and not inferred from resin composition alone. RoHS compliance does not require modification because the resin is not intentionally doped with lead, cadmium, mercury, hexavalent chromium, PBB, or PBDE.
| Test or regulatory area | Designation | Typical control point |
|---|---|---|
| Film tensile properties | ASTM D638-14 | Crosshead speed 25 mm/min at 23 °C |
| Apparent lap shear strength | ASTM D1002-19 | 2024-T3 aluminum, bondline 0.15 mm |
| Density | ISO 1183-1 | 1.10 g/cm³ |
| Neutral salt spray resistance | ASTM B117-19 | Scribe creep ≤3 mm after 500 h |
| Volatile organic compound determination | ISO 11890-2 | Formulation-specific |
When Butvar B-74 replaces Butvar B-76 in an existing solvent-borne primer, the formulator should first lower solids by 5–10 wt% to compensate for the higher solution viscosity and then adjust the solvent blend to maintain a VOC level below the target limit of ISO 11890-2. In air-atomized spray application on steel, dry film thicknesses of 15–25 μm are achievable without sagging when the formulation is adjusted to 20–25 s Ford cup 4 at 25 °C. Crosslinked films exhibit better solvent resistance than thermoplastic films, as shown by methyl ethyl ketone double-rub resistance above 100 cycles in a laboratory comparison. However, published data for this specific configuration is limited to internal supplier evaluations and should not be extrapolated to field exposure.