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Anhui Liwei Chemical Co., Limited.

Butvar B-90

    • Product Name: Butvar B-90
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
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    Specifications
    HS Code 403649
    Product Name Butvar B-90
    Chemical Family Polyvinyl Butyral (PVB)
    Cas Number 63148-65-2
    Physical Form Fine white powder
    Average Molecular Weight Mw 90,000 g/mol
    Glass Transition Temperature 72 °C
    Specific Gravity 1.1 at 25 °C
    Refractive Index 1.49
    Hydroxyl Content 18-20% as PVOH
    Acetate Content 0-1.5%
    Butyral Content 80-82%
    Solution Viscosity 2000-4000 cP (15% in methanol at 25 °C)

    As an accredited Butvar B-90 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Butvar B-90 polyvinyl butyral resin is supplied as free-flowing powder in 25 kg multiwall paper bags with polyethylene liner.
    Container Loading (20′ FCL) 20′ FCL: palletized bags of Butvar B-90 loaded securely, protected from moisture and heat, ensuring safe transport.
    Shipping Butvar B-90 (polyvinyl butyral resin) ships as a non-hazardous powder in sealed multi-wall bags or fiber drums. Keep containers dry and away from heat, sparks, and open flames. Avoid dust accumulation; ground and bond equipment during transfer. Include safety data sheet and proper labeling per transportation regulations.
    Storage Store Butvar B-90 in a cool, dry, well-ventilated area, away from heat, open flames, and strong oxidizing agents. Keep containers tightly closed when not in use to prevent moisture pickup and contamination. Avoid generating dust; ground and bond containers during transfer. Follow manufacturer’s shelf-life guidelines for optimal performance.
    Shelf Life Shelf life for Butvar B-90 is typically two years when stored in original, unopened containers in cool, dry conditions.
    Application of Butvar B-90

    On 2024-T3 clad aluminium and hot-dip galvanized steel substrates destined for multi-layer aerospace, architectural, or automotive refinish coating systems, a two-component poly(vinyl butyral) etch primer is applied as the corrosion-inhibiting pretreatment layer prior to epoxy or polyurethane intermediate coats. In this configuration, Butvar B-90 is incorporated at 6.0–9.0 wt% of the base component, while phosphoric acid at 85% concentration is added at 3.0–4.5 wt% of the total mixed primer immediately before spray application. The base component also contains zinc phosphate at 6.0–9.0 wt%, an inert extender such as talc at 2.0–4.0 wt%, and a solvent blend of methyl ethyl ketone, isopropanol, and toluene as the balance. Compliance is anchored to SAE AMS-C-8514 (formerly MIL-C-8514C) and SSPC-Paint 27, with salt-spray evaluation performed according to ASTM B117 or ISO 9227; the wash primer film itself is not classified as a standalone barrier layer, and corrosion resistance values are referenced to the complete specified topcoat stack rather than to the catalyst-bearing primer alone. Production-scale mixing employs a pressure-pot spray unit fitted with a 1.8–2.2 mm fluid nozzle and air-cap pressure of 0.20–0.30 MPa; wet film is deposited at 20–35 μm to yield a dry film of 8–13 μm after 15–30 min of solvent flash at 20–30 °C. The pot life of the catalyzed material is 6–8 h at 25 °C; beyond this window, progressive hydroxyl-mediated thickening and loss of acid reactivity produce an uneven, low-adhesion film that cannot be corrected by solvent addition. Electrostatic rotary atomizers are rarely specified for this fluid class because the phosphoric acid component imposes an unmanageable conductivity penalty on charged delivery systems. End products include pretreatment of aerospace skins prior to MIL-PRF-23377 epoxy primer, automotive refinish spot repairs, architectural aluminium extrusions before polyester powder topcoats, and structural steel assemblies where overcoating is delayed by several days.

    ComponentFunction in Base ComponentWeight FractionAnchoring Specification / Test Method
    Butvar B-90Film-forming binder6.0–9.0 wt%SAE AMS-C-8514
    Zinc phosphateInhibitive pigment6.0–9.0 wt%SSPC-Paint 27
    TalcExtender / sag control2.0–4.0 wt%ASTM D520 for zinc dust; talc per manufacturer particle size data
    Phosphoric acid (85%)Catalyst / surface etch3.0–4.5 wt% of total mixed primerSAE AMS-C-8514

    What Limits Binder Burnout Ramp Rate in X7R and C0G Multilayer Ceramic Capacitor Tape?

    Dielectric green tapes for multilayer ceramic capacitors—whether X7R/X5R formulations based on calcined barium titanate or C0G formulations based on rare-earth titanates—rely on high-molecular-weight PVB as the primary thermoplastic binder because its glass transition of 72–78 °C and hydroxyl content of 18.5–20.5% (reported as poly(vinyl alcohol) equivalent per Eastman technical data) deliver the green edge-strength and clean pyrolysis profile required in thin-layer stacking. In production, Butvar B-90 is compounded at 5.0–12.0 phr per 100 parts of calcined dielectric powder, with a plasticizer such as butyl benzyl phthalate at 1.5–4.0 phr; the slip is let down to 40–55 wt% solids in a 60:40 methyl ethyl ketone:ethanol solvent blend, yielding a Brookfield viscosity of 1,500–6,000 mPa·s at 25 °C suitable for doctor blade casting. Compliance obligations for dielectric powder classification derive from EIA-198 (which defines C0G, X7R, and X5R temperature characteristics), capacitor-level performance from IEC 60384-22 for Class 2 fixed surface-mount MLCCs, and material restrictions from RoHS Directive 2011/65/EU with Delegated Directive (EU) 2015/863. Tape casting is executed with a doctor blade wet gap of 100–350 μm on a PET carrier moving at 0.5–2.0 m/min; multi-zone drying at 40–90 °C produces green tape thicknesses of 25–150 μm. Lamination stacks are pressed at 60–80 °C and 20–50 MPa. The critical process bottleneck is binder burnout: the temperature ramp from 250–550 °C must not exceed 0.5–2.0 °C/min for tapes thicker than 60 μm, because a steeper ramp generates volatile decomposition products at a rate that exceeds the open-pore permeability of the laminated green body, producing internal delamination. Residual carbon below 0.1 wt% must be achieved before the part enters the 1,100–1,350 °C sintering stage; the high molecular weight of Butvar B-90, while improving punched edge retention and green density, extends the burnout plateau by approximately 15–30 min compared with lower-molecular-weight PVB grades. Published data specific to multilayer stacks exceeding 300 layers using this exact binder grade is limited; burnout profiles must be validated by thermogravimetric analysis per ASTM E1131 on each new tape thickness and layer count. End products include X7R and C0G MLCCs for automotive engine-control modules, portable electronics, and high-frequency modules, as well as LTCC substrates and ceramic packages.

    ParameterMeasured Range / ConditionEquipment or Test Method
    Butvar B-90 addition5.0–12.0 phr on 100 parts dielectric powderWeighing / dispersion audit
    Slip solids40–55 wt%Brookfield viscometer, 25 °C
    Doctor blade wet gap100–350 μmTape casting line, flatness gauge
    Drying zone temperature40–90 °CMulti-zone forced-air dryer
    Burnout ramp0.5–2.0 °C/min to 550 °CASTM E1131 (TGA)
    Sintering temperature1,100–1,350 °CBox or tunnel kiln, shrinkage audit

    Because flexible packaging converters running high-speed flexographic and gravure presses at 120–180 m/min on biaxially oriented polypropylene and polyethylene terephthalate films frequently encounter print delamination on metallized or slip-treated surfaces, Butvar B-90 is used as a co-binder to raise inherent substrate adhesion without shifting the pigment dispersion window of the ink concentrate. In a solvent-based flexographic ink, the resin is added at 1.5–5.0 wt% of the total liquid formulation, paired with nitrocellulose at a ratio of 1:2 to 1:4 PVB:NC on solids; the combined binder level is held at 8–15 wt%, with organic pigment at 10–20 wt% and a solvent blend of ethyl acetate, ethanol, and propyl acetate at 60–75 wt%. Ink manufacture proceeds through a two-stage process: pigment predispersion in a bead mill or three-roll mill at 35–45 °C, followed by let-down at low shear to avoid nitrocellulose degradation. Press-side, the ink is adjusted to a Zahn #2 cup efflux time of 18–25 s; Butvar B-90 at the upper addition range raises viscosity disproportionately, which limits its use in low-viscosity high-definition flexographic work but is advantageous in gravure lamination inks where resin content improves bonding to aluminium-metallized PET. The high hydroxyl content of Butvar B-90 also slows solvent release through hydrogen bonding; if ink is shipped in closed containers above 40 °C, viscosity drift can occur as the resin sorbs ambient humidity from the headspace. Compliance is governed by EU Framework Regulation (EC) 1935/2004, Good Manufacturing Practice Regulation (EC) 2023/2006, the EuPIA Suitability List, and Swiss Ordinance SR 817.023.21; these instruments control migration limits and excluded-substance lists but do not classify Butvar B-90 for direct food-contact surfaces, so the printed ink film is restricted to the non-food-contact side of packaging or to laminations with a functional barrier layer. End products include surface-print and lamination inks for snack packaging, shrink-sleeve labels on PVC, and aluminium-metallized PET film for coffee pouches.

    When Plasticizer Partitioning Outpaces Interlayer Adhesion Targets in ECE R43 Laminates

    Automotive and architectural laminated glass interlayers are produced from PVB resin plasticized with triethylene glycol bis(2-ethylhexanoate) (3G8) or an equivalent linear ester; in this use, Butvar B-90 is the base polymer charged at 100 parts by weight, with plasticizer added at 25–40 phr, an adhesion control salt such as potassium formate at 0.01–0.05 phr, UV stabilizer at 0.1–0.5 phr, and antioxidant at 0.05–0.2 phr. Compliance paths for finished laminated glazing include ISO 12543-2:2021 for architectural safety glass, UN ECE R43 for automotive safety glazing, ANSI Z26.1 for North American vehicle glazing, and GB 9656-2021 for the Chinese market. Compounding is performed in a high-intensity mixer at 50–90 °C, followed by twin-screw extrusion at barrel temperatures of 150–190 °C through a slot die; the melt is then calendered and embossed to thicknesses between 0.38 mm and 1.52 mm. The defining processing boundary is moisture: between compounding and glass lamination, the film must be conditioned at 20–25 °C and 20–35% RH to reach an equilibrium moisture content of 0.35–0.55 wt%; below this range, impact adhesion falls below the mean break height criterion of ISO 12543-2, and above this range, visual edge bubbling occurs during autoclave cycling. The glass-PVB-glass stack is pre-pressed at 60–90 °C then autoclaved at 120–140 °C and 1.1–1.3 MPa for 30–90 min. The high hydroxyl content of Butvar B-90 increases equilibrium moisture uptake relative to lower-hydroxyl grades, which tightens the usable plasticizer range at the low end; plasticizer partitioning into the adjacent poly(ethylene terephthalate) backsheets or photovoltaic cell encapsulant layers can shift the effective plasticizer content of the interlayer over time, and this migration must be confirmed by accelerated damp-heat testing per IEC 61215 before module qualification. End products include vehicle windshields, side and roof glazing, architectural laminated glass for facades and skylights, and PVB-based photovoltaic encapsulant films; published data for the specific use of Butvar B-90 in thin-film photovoltaic module encapsulation is limited, as lower-hydroxyl grades are sometimes preferred to reduce moisture uptake in high-humidity installations.

    Nitrocellulose Sealer Modification and Solvent Release Profiles on Hardwood Substrates

    Cabinet and furniture finishing lines that use nitrocellulose lacquers add Butvar B-90 at 4–8 wt% of the total lacquer formulation to raise alcohol resistance and sanding smoothness on open-grain hardwoods such as oak and ash. Within the lacquer solids, the PVB share is typically 5–10 wt%, with nitrocellulose at 35–45 wt%, alkyd or maleic resin at 10–20 wt%, plasticizer at 5–10 wt%, and solvents comprising n-butyl acetate, ethyl acetate, ethanol, and toluene as the balance. Finish testing follows ASTM D3359 for crosscut adhesion, ASTM D1640 for dry-hard and dry-to-sand times, ISO 1522 for König pendulum hardness, and ASTM D4366 for damping hardness; these test methods are applied to sealed panels rather than to the PVB resin alone. Manufacturing is carried out by cold-cut dissolution in a high-speed disperser at 600–1000 rpm, with bulk temperature held below 40 °C to prevent nitrocellulose destabilization. Application is executed with HVLP or air-assisted airless equipment at fluid pressure of 0.15–0.30 MPa, producing a dry film of 25–50 μm per coat; re-coat intervals are extended by the hydrogen-bonded solvent fraction in Butvar B-90, and forced-air drying above 60 °C risks solvent blistering unless the sealer is formulated with a slower tail solvent such as propylene glycol methyl ether acetate. On production lines, batch-to-batch variance in the PVB hydroxyl content within the 18.5–20.5% specification band shifts sanding softness by a measurable degree; mills that run tight incoming inspection on hydroxyl number reduce rework from telegraphing under subsequent polyester topcoats. End products include furniture sanding sealers, cabinet topcoats, interior wood trim finishes, and edge sealers for medium-density fibreboard components.

    Slot-Die Coated Hot-Melt Adhesive Film Stability at Prolonged Barrel Residence Times

    In textile and automotive interior lamination lines, PVB-based hot-melt adhesive films are specified where a high glass-transition resin is needed to prevent blocking of the film on the release liner during storage and to maintain cohesive strength after lamination. Butvar B-90 is compounded at 20–45 wt% with rosin ester tackifiers at 20–35 wt%, a liquid plasticizer such as butyl benzyl phthalate at 10–20 wt%, a microcrystalline wax at 0–5 wt%, and a phosphite antioxidant at 0.1–0.5 phr. Adhesive performance is specified by ISO 4587:2003 for tensile lap-shear strength and ASTM D903 for flexible-to-flexible peel; regulatory compliance under REACH Regulation (EC) 1907/2006 applies to the plasticizer and tackifier package rather than to the PVB polymer itself. Melt compounding is performed in a co-rotating twin-screw extruder with an L/D ratio of 40:1 at barrel temperatures of 130–180 °C; the melt is then filtered through a screen pack of 100–250 μm and coated through a slot die at 150–180 °C onto a siliconized release liner. The process boundary is thermal residence time: at the upper temperature of 180 °C, prolonged screw residence beyond 30–40 min initiates measurable yellowing and acetaldehyde evolution from the poly(vinyl butyral) backbone, so line shutdowns require rapid purging with a low-melting polyethylene purge compound. The high melt viscosity of Butvar B-90 also restricts slot-die coat weight at speeds above 20 m/min; coater trials at higher line speeds typically require a viscosity modifier or a minor fraction of lower-molecular-weight PVB. End products include automotive interior lamination films for headliners and door panels, textile transfer adhesives, and edge-bonding films for footwear; published data on this specific Butvar B-90 hot-melt configuration is limited, and pilot trials on the target slot-die setup are required before scale-up.

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    Certification & Compliance
    More Introduction

    Polyvinyl butyral resin grade Butvar B-90 (CAS 63148-65-2) is manufactured by Eastman Chemical Company as a free-flowing white powder. The polymer is a terpolymer of vinyl butyral, vinyl alcohol, and vinyl acetate; the vinyl butyral segment is approximately 80 wt%, hydroxyl content is 18.5–20.5 wt% expressed as polyvinyl alcohol, and acetate content is ≤2.5 wt%. Typical weight-average molecular weight is 90,000 g/mol by gel permeation chromatography, and the glass transition temperature is 72–75°C by differential scanning calorimetry per ASTM D3418. A 15 wt% solution in 60:40 toluene/ethanol at 25°C yields a Brookfield viscosity of 600–1,000 mPa·s per ISO 2555. Relative to higher-viscosity PVB grades such as Butvar B-72, B-90 permits higher application solids in gravure and roller coating while retaining sufficient binder cohesive strength. Relative to lower-hydroxyl PVB resins, B-90 provides greater reactive site density for crosslinked film formation but also greater moisture sensitivity.

    Typical published data for Butvar B-90 resin
    PropertyValueMethod/designation
    Physical formFree-flowing white powderVisual inspection
    Weight-average molecular weight90,000 g/molGel permeation chromatography
    Solution viscosity, 15 wt% in 60:40 toluene/ethanol at 25°C600–1,000 mPa·sISO 2555, Brookfield-type rotational viscometer
    Hydroxyl content, wt% as polyvinyl alcohol18.5–20.5ASTM D1396
    Acetate content, wt%2.5ASTM D1396
    Butyral content, wt%77–81 calculatedBy difference
    Specific gravity1.10ASTM D792
    Glass transition temperature72–75°CASTM D3418

    What Limits Solvent Loading and Viscosity in Butvar B-90 Solution Preparation?

    Solvent selection controls apparent viscosity, drying rate, and film clarity. B-90 dissolves in ketones such as methyl ethyl ketone, in esters such as ethyl acetate, and in alcohol/aromatic hydrocarbon blends. The standard control solution is 15 wt% solids in 60:40 toluene/ethanol. Above 18–20 wt% solids, viscosity rises sharply and shear thinning becomes pronounced; on a Brookfield viscometer at 20 rpm, apparent viscosity can double for every 2–3 wt% increase in solids. Production compounding in a 100–200 L vessel with a Cowles-type high-shear disperser at 8–12 m/s tip speed requires pre-wetting the powder in ethanol before adding the toluene fraction. Direct addition to toluene-rich media forms translucent agglomerates; these require 30–60 min additional dispersion and increase filtration time through a 100 µm bag filter. Water content in the solvent system should remain below 2 wt% because water acts as an anti-solvent for the butyral segments and produces haze. Storage stability is improved by nitrogen blanketing and storage below 30°C; oxidative yellowing can be retarded by adding 0.05–0.20 wt% butylated hydroxytoluene based on resin solids. The solubility limit for this grade in purely aliphatic hydrocarbon solvents is low; maintaining at least 20 wt% aromatic or ketone co-solvent is required to avoid precipitation during solvent evaporation.

    In solvent-based gravure and flexographic ink systems, B-90 is added at 2–6 wt% of the liquid ink as a co-binder with nitrocellulose or polyurethane. The resin improves film toughness and adhesion to corona-treated polyethylene and polypropylene; adhesion is evaluated by tape peel per ASTM D3359 after 24 h at 23°C. The hydroxyl content allows post-print crosslinking with polyfunctional isocyanates at an NCO:OH ratio of 0.8–1.2. The higher molecular weight of B-90, relative to low-viscosity PVB grades, increases ink transfer and reduces misting on high-speed presses, but it also raises apparent viscosity at press-side shear rates and requires stronger solvent blends.

    Ceramic tape-casting operations employ B-90 at 4–8 wt% resin solids relative to ceramic powder in non-aqueous slip. The slip typically contains 55–65 wt% ceramic solids, 35–45 wt% solvent, and the resin as binder. The resin adsorbs onto barium titanate particle surfaces and prevents particle-to-particle aggregation under the shear field of the doctor blade. Tape cast through a 200–400 µm gap at 0.8–1.5 m/min produces green sheets; after drying, green tensile strength is characterized by ASTM D638 but varies with plasticizer level and residual solvent. B-90 provides higher green sheet tensile strength than low-molecular-weight PVB grades because of increased chain entanglement. Binder burnout occurs before densification; thermogravimetric analysis in air at 10°C/min per ASTM E1131 shows decomposition onset near 250°C and residual ash ≤0.1 wt% at 600°C. Incomplete burnout above 450°C leaves carbonaceous residue that can increase dielectric loss tangent; production kiln profiles therefore hold the charge at 350–400°C for 1–2 h before sintering.

    Plasticizer uptake dictates film elongation and low-temperature flexibility.

    Unplasticized B-90 film is brittle at room temperature because its glass transition is 72–75°C. Plasticization with 20–40 phr dibutyl phthalate, dioctyl adipate, or triethylene glycol bis(2-ethylhexanoate) lowers the glass transition into the 30–45°C range and increases elongation at break to 200–300% when tested per ASTM D638 at 23°C and 50% RH. The exact depression follows the Fox relationship; specific values for a given plasticizer-polymer pair should be confirmed by differential scanning calorimetry and dynamic mechanical analysis because published data for this exact configuration is limited. Plasticizer exudation is avoided when the plasticizer solubility parameter is within approximately 1.5 MPa^0.5 of the resin. At relative humidity above 60%, pre-drying of the resin at 40–50°C for 4–6 h is required to prevent bubble formation during film casting. Films laminated under 10–15 bar at 90–120°C bond to glass; final adhesion is measured by ISO 2409 crosshatch testing. Strong mineral acids are incompatible with B-90 at elevated temperatures because the acetal linkages hydrolyze, releasing butyraldehyde and reducing molecular weight. For thermoplastic melt compounding, B-90 is pre-mixed with plasticizer in a high-intensity mixer at 60–80°C before feeding to a co-rotating twin-screw extruder with L/D 40 and barrel temperatures from 120 to 160°C. Vented barrels remove residual ethanol; vacuum levels below 0.08 MPa prevent bubbles in strand pelletization. Residence time above 120 s at temperatures above 180°C causes yellowing and crosslinking.

    Solvent-borne wash primers use B-90 as the film former in a two-component acid-catalyzed system. The resin is dissolved at 10–15 wt% solids in a methyl ethyl ketone/ethanol mixture; zinc tetroxychromate or zinc phosphate is dispersed as the corrosion-inhibiting pigment, and phosphoric acid is added at 0.5–1.5 wt% of total formulation to activate the substrate. Acidified formulations require mixing below 25°C because phosphoric acid accelerates acetal hydrolysis; pot life is controlled by acid concentration and is typically limited to 8–12 h. The primed film is applied by spray to dry film thicknesses of 8–15 µm. After 7 days at 23°C and 50% RH, crosshatch adhesion per ISO 2409 is typically class 0–1 on aluminum and galvanized steel. Amine-based anti-flash additives are not recommended because they shift pH and destabilize the acid-catalyzed film. Use of chromate pigments is subject to authorization in the EU under REACH; non-chromate substitutes may require adjustment of the resin-to-pigment ratio to maintain salt spray performance.

    Burnout Profile and Ash Residue in Co-fired Ceramic Laminates

    During co-firing of multilayer ceramic capacitors, the organic phase must be removed before densification. Butvar B-90 decomposes in a two-stage process under flowing air. The first mass loss begins near 250°C and is attributed to elimination of hydroxyl and acetate side groups; the second stage, oxidative backbone degradation, completes before 450°C at a ramp rate of 10°C/min per ASTM E1131. Residual ash at 600°C is ≤0.1 wt%, which is suitable for co-fired electrode systems. A faster ramp of 20°C/min can leave carbonaceous residue; this carbon can reduce insulation resistance and raise dielectric loss. Production kiln profiles hold the charge at 350–400°C for 1–2 h before the high-temperature sintering segment. The low ash content is a point of differentiation from lower-purity PVB resins and from acrylic binders that may leave higher cation residues.

    When Butvar B-90 Replaces Lower-Hydroxyl PVB in Structural Adhesive Formulations

    When B-90 is substituted for a PVB grade with hydroxyl content 12–14 wt% in a two-part isocyanate-cured adhesive, the higher hydroxyl density increases crosslink probability and shortens gel time at constant NCO:OH ratio. A formulation at 20 wt% resin solids in methyl ethyl ketone with hexamethylene diisocyanate trimer and 0.05 wt% dibutyltin dilaurate exhibits a gel time of 45–60 min at 23°C, whereas the lower-hydroxyl resin gels in 90–120 min under the same mixing protocol. Lap shear strength on chromic-acid-etched aluminum per ASTM D1002 is formulation-dependent; published data for this exact B-90/aluminum configuration is limited, but cohesive failure within the PVB phase is generally observed when the adhesive-to-substrate bond is adequate. The same hydroxyl density raises water uptake; cured films immersed in water at 40°C for 7 days can lose 10–20% of initial tensile strength unless a silane adhesion promoter is used. The operational boundary is a maximum service humidity of 80% RH for permanently loaded joints without additional water-resistant primer.