Products

Products

Anhui Liwei Chemical Co., Limited.

PVB WW-A-60

    • Product Name: PVB WW-A-60
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
    • CONTACT NOW
    Specifications
    HS Code 487598
    Product Name PVB WW-A-60
    Chemical Name Polyvinyl butyral
    Cas Number 63148-65-2
    Appearance White free-flowing powder
    Viscosity 60 ± 10 seconds (Tu-4 cup, 10% ethanol solution, 25°C)
    Molecular Weight Approximately 60,000 g/mol (viscosity-average)
    Hydroxyl Content 18.0 - 20.0 wt%
    Butyral Content 80.0 - 82.0 wt%
    Acetate Content ≤ 2.0 wt%
    Water Content ≤ 0.5 wt%
    Ash Content ≤ 0.1 wt%
    Density 1.08 - 1.12 g/cm³
    Glass Transition Temperature 70 - 80 °C
    Softening Point 100 - 110 °C
    Solubility Soluble in ethanol, methanol, acetone, and dichloromethane; insoluble in water

    As an accredited PVB WW-A-60 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing PVB WW-A-60 is supplied as a white powder in 25 kg multi-layer paper bags with an inner polyethylene liner.
    Container Loading (20′ FCL) 20′ FCL loading of PVB WW-A-60: palletized, shrink-wrapped bags/drums, secured with bracing, moisture-protected, properly ventilated for safe transport.
    Shipping PVB WW-A-60 is polyvinyl butyral resin, typically shipped as a non-hazardous, non-regulated powder or granule. It is packed in moisture-proof bags or fiber drums, protected from humidity and heat. Standard freight, truck, or sea container transport is suitable, with handling to avoid tearing and contamination.
    Storage Store PVB WW-A-60 in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep the original container tightly sealed to prevent moisture absorption and contamination. Avoid direct sunlight and strong oxidizing agents. Maintain stable temperature, ideally below 30°C, and follow first-in, first-out rotation to preserve resin quality and shelf life.
    Shelf Life PVB WW-A-60 has a typical shelf life of 2 years when stored unopened in a cool, dry, tightly sealed container.
    Application of PVB WW-A-60

    In laminated safety glass interlayer production, PVB WW-A-60 is dry-blended at 72–78 parts by mass with 22–28 parts of triethylene glycol bis(2-ethylhexanoate) or dihexyl adipate, with an adhesion control salt added at 0.02–0.10 parts and a hindered amine light stabiliser at 0.10–0.30 parts. The blend is fed into a counter-rotating twin-screw extruder with L/D 44:1, vented under −0.08 MPa, and cast through a slot die at melt temperature 180–210 °C onto chill rolls set at 15–25 °C. The resulting sheet is conditioned to 0.30–0.45 wt% moisture before lamination. Glass layup is de-aired through nip rolls, then processed in an autoclave at 12–14 bar and 135–145 °C for 30–90 min; pummel adhesion values typically fall in the 3–7 range under EN ISO 12543-2:2021. Terminal finished product types include automotive windshields under ECE R43, architectural laminated safety glass under EN ISO 12543-2:2021, and anti-intrusion glazing under EN 356. Operational boundaries include sheet storage below 25 °C and 40% RH; moisture above 0.45 wt% produces autoclave-edge bubble defects, while overdried sheet below 0.20 wt% reduces melt flow at the glass edges during autoclave consolidation.

    What Limits Solvent Retention in Flexographic Ink Binders on Coextruded Films?

    PVB WW-A-60 is incorporated into solvent-borne flexographic and gravure ink systems at 5–9 wt% of total ink formulation for flexo and 10–15 wt% for gravure, corresponding to 35–55 wt% of the total resin solids in a co-binder network with polyurethane or nitrocellulose. The resin is dissolved in an ethyl acetate/ethanol blend at 80:20 to 70:30 by mass in a high-shear dissolver operating at 18–22 m/s tip speed, then ground on a bead mill at 2,000–2,500 min⁻¹ until a Hegman grind of 5–6 is achieved; final printing viscosity is adjusted to 18–25 s on an ISO 2431 3 mm cup at 23 °C. Compliance is governed by the EuPIA Good Manufacturing Practice, REACH 1907/2006 Annex XVII, and FDA 21 CFR 175.105 for indirect food-contact surface printing where applicable; residual solvent testing follows ISO 11890-2. Terminal finished product types include surface-printed BOPP pouches, PET lidding films, PA vacuum bags, and shrink sleeve labels. The critical processing restriction is solvent balance: increasing ethanol above 60 wt% of the solvent phase can raise solution cloud point and cause binder gel-body formation on cylinder surfaces, while ketone-rich letdown solvent is avoided because it reduces nitrocellulose compatibility and increases retained solvent after ovens set at 60–80 °C with air velocity 8–12 m/s.

    In acid-catalysed wash primer systems applied to degreased steel and aluminium, PVB WW-A-60 is dissolved at 4–7 wt% of the primer mass in a cold mixing vessel, with 2–4 wt% of 85% phosphoric acid and 5–12 wt% of zinc tetroxychromate or strontium chromate dispersed as the inhibitive pigment. The primer is applied by air-assisted spray equipment with nozzle size 1.2–1.4 mm and fluid pressure 0.8–1.2 bar, giving a dry film thickness of 8–15 μm. Corrosion system qualification falls under ISO 12944-5:2019 for C3 and C4 corrosivity categories, with cross-cut adhesion evaluated to ISO 2409:2020 class 0–1; SSPC-Paint 27 provides the relevant etch primer performance framework. Terminal finished product types include aircraft aluminium pretreatment skins, automotive refinish metal parts, and structural steel members in marine environments. Pot life after two-component mixing is limited to 8–12 h at 20 °C because prolonged acid contact hydrolyses the PVB backbone; amine-based hardeners must be excluded from the same mixing equipment due to premature salt formation and viscosity collapse.

    Ceramic Green Tape Slurry Viscosity and Burnout Kinetics

    In dielectric and LTCC green tape manufacturing, PVB WW-A-60 functions as the primary thermoplastic binder at 6–12 wt% of total slurry mass, with a plasticizer such as dibutyl phthalate or butyl benzyl phthalate added at 25–35 wt% of binder mass. The slurry is prepared in a ball mill using 1 mm yttria-stabilised zirconia media for 18–24 h, filtered through a 10 μm absolute filter, and de-aired under 15–25 kPa vacuum before tape casting. Doctor blade gap is set to 80–300 μm, and the drying tunnel is zoned from 70 °C to 95 °C with progressively reduced solvent vapour pressure; the dried green tape is calendered at 60–75 °C and 0.4–0.8 MPa to control density. Lamination of printed layers uses 65–75 °C platen temperature and 1,000–3,000 psi for 10–20 min, followed by binder burnout at 0.5–1.5 °C/min to 350–450 °C with a 2–4 h hold to keep residual carbon below 0.2 wt%. Terminal finished product types include multilayer ceramic capacitors under IEC 60384-1, LTCC substrates, and oxygen sensors. RoHS 2011/65/EU Annex II and REACH 1907/2006 Annex XVII apply to the final ceramic article when exported to the EU. The primary failure mode is edge curling caused by skin formation when the drying air velocity exceeds 2.5 m/s during the first zone; binder exudation is observed when lamination pressure exceeds 3,500 psi at platen temperatures above 80 °C. Published data for PVB WW-A-60 in tape casting at deposition thickness below 10 μm is limited, so pilot-scale qualification is required before ultra-thin MLCI production.

    Representative tape casting slurry window for PVB WW-A-60
    VariableLower boundUpper bound
    Binder on total slurry mass6 wt%12 wt%
    Plasticizer on binder mass25 wt%35 wt%
    Solvent mass fraction50 wt%65 wt%
    Casting viscosity at 25 °C, 20 s⁻¹1,200 mPa·s3,800 mPa·s
    Drying zone air temperature70 °C95 °C
    Burnout ramp rate0.5 °C/min1.5 °C/min

    Compression-moulded phenolic prepreg for aircraft interior panels and friction components incorporates PVB WW-A-60 at 5–15 parts per hundred resin as a toughening modifier, reducing brittle crack propagation in cured novolac networks. The resin is dissolved in an ethanol/MEK mixture, then used to impregnate glass or aramid fabric; B-staging is conducted at 90–110 °C to achieve a defined flow window before final compression moulding at 140–160 °C and 10–20 MPa. Mechanical qualification follows ASTM D638-14 for tensile and ASTM D790-17 for flexural properties; aircraft interior flammability is evaluated under FAR 25.853(a). Terminal finished product types include aircraft seat shells, interior panels, abrasive wheel backing, and heavy-duty friction linings. The incompatibility boundary is with hexamethylenetetramine-activated systems above 12 phr PVB, where die-filling viscosity drops too steeply and flash control becomes unstable.

    When Thin-Film BIPV Modules Use PVB Encapsulant, Lamination Pressure and Edge Sealing Are Process-Defined

    PVB WW-A-60 is converted into encapsulant sheet at 0.76–1.14 mm thickness for thin-film BIPV modules, where the resin sheet is placed between the backsheet and the photovoltaic glass without a liquid adhesive. Vacuum lamination is carried out at 145–155 °C platen temperature, with chamber evacuation to 30–60 kPa before membrane pressure is applied, and total cycle hold of 10–20 min. The module must satisfy IEC 61215-1:2021 and IEC 61730-2:2016, with damp-heat testing at 85 °C/85% RH for 1,000 h used to qualify edge seal integrity. Terminal finished product types include building-integrated photovoltaic facades, spandrel glass modules, and thin-film solar canopies. The primary limitation is open-edge moisture ingress; if butyl edge sealant is not mechanically compressed into the laminate edge, PVB plasticizer migration and delamination can occur within the first 500 h of damp-heat exposure. Laminators calibrated with EVA at 140 °C must not assume the same cure behaviour because PVB requires higher temperature and vacuum ramp profile adjustment.

    Structural PVB Film Lamination Without Autoclave Requires Reduced Plasticizer Migration

    For non-automotive glass-to-metal and glass-to-polycarbonate bonding, PVB WW-A-60 is cast into adhesive film at 0.25–0.76 mm thickness using 15–25 wt% plasticizer on resin mass, selected to lower storage modulus without producing open-time edge squeeze. Hot-press lamination is performed at 120–135 °C and 0.5–1.0 MPa for 15–30 min, with a heated platen cool-down step to 40 °C under pressure to control shrinkage. Lap shear of bonded aluminium specimens is tested to ASTM D1002-10 and ISO 4587:2003; adhesion to powder-coated aluminium is verified by cross-cut under ISO 2409:2020 class 0–1. Terminal finished product types include laminated display cases, protective glazing for rail interiors, and transparent architectural partitions. Published creep data for PVB films on powder-coated aluminium at sustained shear above 0.5 MPa is limited, so film thickness and plasticizer level must be qualified by application-specific lap shear ageing rather than by extrapolation from glass-to-glass data. The processing boundary is plasticizer migration when the film contacts polycarbonate: bisphenol-A polycarbonate is incompatible with high phthalate loads above 25 wt% and develops surface hazing after 72 h at 60 °C.

    Free Quote

    Competitive PVB WW-A-60 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

    Inquiry

    Get Free Quote of Anhui Liwei Chemical Co., Limited.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    PVB WW-A-60 is a polyvinyl butyral resin supplied as free-flowing granules with a water-white visual specification and a mid-range solution viscosity profile. The polyvinyl butyral backbone is described by CAS Registry No. 63148-65-2; typical commercial PVB resins comprise 11–20 wt% polyvinyl alcohol, 0–2.5 wt% polyvinyl acetate, and the balance polyvinyl butyral as determined by ASTM D1396. The WW designation is controlled by solution color on a platinum-cobalt scale according to ASTM D1209. The A-60 suffix is a manufacturer-specific grade modifier rather than an ISO or ASTM nomenclature element; published data for this specific configuration is limited, and the certificate of analysis should be treated as the controlling source. The primary differentiation from general-purpose PVB is lower initial solution chroma and a narrower viscosity band, while high-hydroxyl PVB grades generally provide higher hydrogen-bond density, higher tensile strength, and greater moisture uptake at equivalent molecular weight.

    On a production-scale dissolver with a 1000 L jacketed vessel and an anchor agitator operated at 30–60 rpm, PVB WW-A-60 is charged into a preblended ethanol/toluene co-solvent system at 20–25 °C, then heated to 40–50 °C for complete solvation. A Cowles blade above 5 m/s tip speed is avoided because entrained microfoam persists in low-color clearcoats. The endpoint is checked with a Brookfield rotational viscometer at 25 °C and 20 min⁻¹; the batch is filtered through a 25 µm bag filter when two consecutive readings are within ±5%. This procedure is adopted for wash primer intermediates because undispersed particles larger than 10 µm create localized adhesion defects on cold-rolled steel.

    Why Does Acidic Hydrolysis Impose a Shelf-Stability Boundary in WW-A-60-Based Wash Primers?

    In SSPC-Paint 27-type metal pretreatment, the PVB component is normally supplied as a base component and activated with phosphoric acid immediately before use. The acetal linkages in PVB WW-A-60 are vulnerable to acid-catalyzed chain scission; viscosity loss in the mixed primer is therefore a direct indicator of backbone hydrolysis. Quality-control panels prepared according to ISO 2409 are used to establish cross-cut adhesion to cold-rolled steel after dry film thickness of 8–15 µm as specified in SSPC-Paint 27. Once the acid activator is added, mixed viscosity should be tracked at 25 °C and 50% relative humidity; a Brookfield viscosity decrease greater than 15% from the initial reading indicates that the batch has exceeded its useful pot life. Exact activation energies for WW-A-60 are not specified in public literature; however, acetal hydrolysis generally follows pseudo-first-order behavior with respect to hydronium ion concentration, and storage above 30 °C or at pH below 2.0 sharply reduces usable life. Strongly alkaline additives and strong oxidizing agents should not be introduced into the acid-activated mixture because they accelerate side reactions and premature film embrittlement.

    In ceramic green tape casting, PVB WW-A-60 serves as a nonaqueous binder for barium titanate or alumina suspensions because its hydroxyl distribution provides adequate interparticle hydrogen bonding without excessive moisture affinity. A typical slurry is compounded in a high-shear disperser at 400–800 rpm, followed by a three-roll mill at a controlled gap of 20–40 µm to eliminate agglomerates. The binder loading is commonly 4–8 wt% of inorganic solids; higher binder content raises green tensile strength but also increases binder burnout residue if the air furnace profile is not staged. Thermogravimetric analysis at 10 K/min under air typically shows major PVB mass loss between 350 °C and 500 °C; the burnout ramp must therefore hold at 250 °C for 60 min before the peak soak to avoid blistering of 50–150 µm green tape. The mid-range viscosity of WW-A-60 permits higher solids loading than high-molecular-weight PVB while retaining enough green strength for automatic handling on single-sheet laminators.

    Solvent Compatibility, Viscosity Thresholds, and Optical Aging in Flexographic Printing Inks

    PVB WW-A-60 dissolves in ethanol, isopropanol, methyl ethyl ketone, and glycol ethers; aromatic hydrocarbons are used as diluents rather than sole solvents. Solvent selection is constrained by the Hansen solubility parameters of PVB, but for this grade the supplier certificate should be used because the residual acetate content shifts solubility in aliphatic systems. In flexographic ink milling, a base resin solution at 25–35 wt% solids is dispersed with pigment using a bead mill at 3000–6000 rpm and a chamber temperature below 45 °C. Viscosity at press side is typically adjusted with a solvent blend of ethanol and n-propyl acetate; a No. 2 Zahn cup reading of 18–25 s at 25 °C is a common target for anilox delivery, but the WW-A-60 certificate of analysis should be used to confirm lot-specific solution rheology. Optical aging is evaluated by accelerated exposure in a QUV chamber according to ISO 4892-3; water-white grades should show lower initial Pt-Co color than general-purpose PVB, but yellowing remains dependent on residual catalyst residues and antioxidant stabilization. Strong oxidizing agents and concentrated mineral acids should be excluded from the solvent system because acetal cleavage and yellowing increase rapidly.

    For laminated glass interlayer compounding, PVB WW-A-60 would be evaluated against plasticized PVB grades rather than solvent-borne coating grades; the A-60 mid-range viscosity is not a direct substitution for high-hydroxyl safety glass interlayers without reformulation. In twin-screw extrusion with L/D ratio 30:1–40:1, barrel zones from 150 °C to 210 °C, and vacuum venting at −0.08 MPa, moisture must be kept below 0.2 wt% because excess moisture produces bubbles and optical haze. Pre-drying at 60 °C for 2–4 h in a desiccant dryer is required if storage relative humidity has exceeded 60%. Melt viscosity and plasticizer uptake are not described by a single test method; dynamic rheology in the linear viscoelastic region at 150 °C under nitrogen can quantify processability. This grade is not recommended as a drop-in replacement for plasticizer-free high-Tg PVB used in structural interlayers because the molecular weight and plasticizer compatibility window must be revalidated by durability testing in accordance with ISO 12543-4.

    When a high-solids gravure ink formulation is reduced to press viscosity, PVB WW-A-60 contributes both pigment wetting and film toughness; however, the formulator must confirm that the active solvent blend does not exceed the resin cloud point. In a closed-loop ink delivery system with a 10 L ink reservoir and gravure cylinder at 120 m/min, lot-to-lot solution viscosity variation above ±10% can shift transfer density and highlight dot gain. Maintaining the resin moisture content below 0.5 wt% before dissolution reduces batch-to-batch variation; this is routinely checked by ISO 3251 volatile determination or Karl Fischer titration after drying.

    Regulatory documentation for PVB WW-A-60 is lot-dependent and requires verification against the supplier safety data sheet because polymer registration status, monomer residuals, and stabilization additives vary by production site.

    Property axisStandard methodTypical differentiation range for PVB grade selection
    Hydroxyl contentASTM D1396General-purpose coatings grades span 11–20 wt% polyvinyl alcohol; higher hydroxyl increases tensile strength and moisture uptake.
    Solution viscosityBrookfield rotational viscometer at 25 °CA 10 wt% solution in 95% ethanol is used; low-viscosity grades fall below 50 mPa·s, mid-range grades commonly fall between 50 mPa·s and 200 mPa·s, and high-molecular-weight grades exceed 200 mPa·s.
    Glass transitionISO 11357-2Plasticizer-free PVB typically falls between 70 °C and 78 °C; plasticizer content depresses Tg in proportion to plasticizer addition.
    Yellowness indexASTM E313Water-white grades are specified for low initial chroma; accelerated UV testing is still required because PVB yellows with residual catalyst and antioxidant depletion.
    Regulation or standardApplicability to PVB WW-A-60Literal control point
    EU REACH EC 1907/2006Polymer registration and SVHC screening under Articles 7 and 33Supplier SDS Section 3 and Section 15
    US FDA 21 CFR 175.105Adhesives and coating components for indirect food contact may be relevant for laminating and ink gradesSupplier food-contact statement and lot-specific migration data where applicable
    RoHS Directive 2011/65/EULead, cadmium, mercury, hexavalent chromium, PBB, and PBDE restrictions for electrical and electronic applicationsXRF screening and wet digestion according to IEC 62321-5
    Plastics Regulation EU 10/2011Overall migration and specific migration limits for plastic materials intended for food contactMigration testing under prescribed food simulants; not assumed for WW-A-60 without supplier confirmation