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Anhui Liwei Chemical Co., Limited.

PVB WW-A-10

    • Product Name: PVB WW-A-10
    • 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 858219
    Product Name PVB WW-A-10
    Chemical Name Polyvinyl Butyral
    Cas Number 63148-65-2
    Molecular Formula (C8H14O2)n
    Molecular Weight 20000-40000
    Appearance White fine powder
    Color White
    Density 1.08-1.15 g/cm³
    Viscosity 5 Ethanol Solution 25 C 10-18 mPa·s
    Butyral Content 70-80%
    Residual Hydroxyl Content 17-23%
    Residual Acetate Content ≤3%
    Softening Point 60-70°C
    Glass Transition Temperature 60-70°C
    Water Absorption 24h 0.4-0.6%
    Solubility Soluble in ethanol, methanol, isopropanol, butanol, glycol ethers and ethyl acetate; insoluble in water and aliphatic hydrocarbons

    As an accredited PVB WW-A-10 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing PVB WW-A-10 is supplied as a free-flowing powder in 25 kg multi-walled paper bags with a polyethylene liner.
    Container Loading (20′ FCL) 20′ FCL: PVB WW-A-10 loaded in bags on pallets, securely stowed and braced for safe transport.
    Shipping Polyvinyl butyral (PVB), grade WW-A-10, is supplied as a free-flowing thermoplastic powder. Ship in dry, sealed, moisture-resistant packaging to prevent caking. Protect from excessive heat and ignition sources. Not regulated as hazardous material under DOT/IMDG; use standard dust-control and industrial hygiene practices during handling and transport.
    Storage Store PVB WW-A-10 (polyvinyl butyral) in a cool, dry, well-ventilated location away from open flames, sparks, and oxidizing agents. Keep containers tightly closed when not in use to prevent moisture absorption and contamination. Avoid direct sunlight, high heat, and humid conditions. Maintain moderate temperatures and use first-in/first-out stock rotation. Keep storage area free of ignition sources.
    Shelf Life PVB WW-A-10 typically has a two-year shelf life from manufacture when stored in a cool, dry place.
    Application of PVB WW-A-10

    In laminated safety-glass interlayer compounding, PVB WW-A-10 is introduced as a polyvinyl butyral binder resin that must be dried to residual moisture below 0.20 wt% before extrusion; moisture above 0.35 wt% produces bubbles, edge clouding, and autoclave delamination. The grade is typically compounded with triethylene glycol di-2-ethylhexanoate or dibutyl sebacate in a co-rotating twin-screw extruder with L/D 30:1 to 40:1, melt temperature 180–220 °C, and a sheet die maintained within ±3 °C of setpoint. Plasticizer loading is adjusted so that the interlayer glass transition temperature falls between 26 °C and 32 °C for automotive glazing; residual hydroxyl content in commercial PVB grades ranges from 11 wt% to 21 wt% and controls glass adhesion through hydrogen bonding, while trace acetate groups below 3 wt% modify solubility and thermal stability. Adhesion control salts, typically magnesium or potassium salts at 50–300 ppm on resin, are introduced to stabilize glass adhesion under humid service conditions. Laminated assemblies are processed through a nip-roll deairing stage at 60–80 °C, followed by an autoclave cure at 120–140 °C and 1.0–1.5 MPa for 30–90 min. Optical quality is assessed under ISO 12543-2, impact and fracture behavior under ECE R43 or ANSI Z26.1, and moisture resistance after immersion in boiling water for 2 h per ISO 12543-4. Haze and yellowness are quantified per ASTM D1003 and ASTM E313. Production-scale failure modes observed on continuous sheet lines include batch-to-batch viscosity drift from hydroxyl content variation, edge tearing when die lip temperature deviates more than ±3 °C, and plate-out on chill rolls when acetate content exceeds the upper specification limit. Because published data for PVB WW-A-10 in high-volume interlayer extrusion is limited, pilot trials on a 25 mm twin-screw extruder with L/D 40:1 are required before transfer to 75 mm production lines.

    Application segmentStandard / clauseTest methodControlled variable
    Laminated safety glass interlayerISO 12543-2Optical defect classesMoisture ≤0.20 wt%
    Automotive laminated glazingECE R43Impact and fractureAutoclave 120–140 °C
    Architectural laminated safety glassANSI Z97.1 / EN 14449Impact classificationInterlayer thickness

    What Limits Ceramic Tape-Casting Binder Burnout in Reducing Atmospheres?

    For non-aqueous tape-casting slurries used in multilayer ceramic capacitors, low-temperature co-fired ceramic substrates, and alumina dielectric tapes, PVB WW-A-10 functions as a thermoplastic binder whose decomposition profile controls green-body burnout and sintered dielectric cleanliness. A representative formulation combines ceramic powder at 55–65 wt% of slurry, PVB WW-A-10 at 6–12 wt% of ceramic solids, dibutyl phthalate or benzyl butyl phthalate as plasticizer at 20–30 wt% of binder, and a phosphate ester dispersant at 0.5–1.5 wt% of ceramic solids in a methyl ethyl ketone/ethanol solvent system. Slurry viscosity is measured on a cone-plate viscometer at 25 °C, with acceptable doctor-blade casting between 1,000 mPa·s and 3,500 mPa·s. Cast green tape is dried at 50–70 °C and tested for tensile strength and elongation per ASTM D882, while binder decomposition is profiled by thermogravimetric analysis per ISO 11358 from 25 °C to 600 °C. PVB decomposition in air begins near 200 °C with side-group elimination and continues through main-chain oxidation, reaching near-complete mass loss by 550 °C; in reducing nitrogen atmospheres, residual carbon can persist beyond 600 °C and levels above 0.05 wt% can degrade dielectric loss and insulation resistance, so staged debinding with controlled oxygen partial pressure is required before sintering. Ash content and alkali-metal residues must be verified because sodium or potassium above 50 ppm may compromise MLCC reliability under AEC-Q200 bias humidity testing. Production bottlenecks include slurry skinning on the doctor blade, binder migration during drying, and variation in green tape thickness when solvent evaporation exceeds 0.8 g/m²·s; these are controlled by adjusting solvent ratio and casting speed. Published data for PVB WW-A-10 in ceramic tape casting is limited, so each ceramic powder lot requires binder burnout profiling and slurry rheology mapping before full-scale casting.

    Solvent-borne wash primers and metal pretreatment coatings use PVB WW-A-10 as the binder component in a single-pack acid-catalyzed system applied to galvanized steel, aluminum, and stainless steel before structural bonding or topcoating. A representative formulation contains PVB WW-A-10 at 5–9 wt% of total liquid, 85% phosphoric acid at 1–3 wt%, zinc chromate or zinc phosphate at 2–4 wt%, and an isopropanol/butanol/toluene solvent blend adjusted for flash point and evaporation rate. The acid component etches the metal surface and forms a phosphate conversion layer, while PVB WW-A-10 provides adhesion interphase integrity and resistance to topcoat solvent attack. Mixed primer has a pot life of 6–12 h before viscosity rise and pigment settling require re-agitation; closed mixing vessels and continuous slow-speed stirring reduce moisture uptake. The primer is applied at 5–10 μm dry film thickness, dried at 20–25 °C for 15–30 min, and then overcoated within 24 h. Adhesion is verified per ASTM D3359 cross-cut tape test after 24 h; salt-spray resistance is evaluated per ISO 9227 on scribed panels; humidity resistance is assessed per ASTM D4585. Chromate-bearing formulations face REACH Annex XVII restrictions and require authorization or replacement by zinc phosphate or organosilane inhibitors. PVB WW-A-10 contributes no direct electrochemical inhibition; its main function is to bind the acid-reactive pigment and maintain film integrity during the conversion process. Production observations include nozzle clogging when phosphoric acid reacts prematurely with zinc pigment and dry film delamination if relative humidity during drying exceeds 70%; these are managed by component order-of-addition and targeted solvent evaporation profile.

    Solvent-Borne Gravure and Flexographic Ink Binder Function

    In multi-layer flexible packaging inks, PVB WW-A-10 is dissolved in an ethanol/ethyl acetate/n-propanol blend and used as a film-forming binder for lamination inks on corona-treated biaxially oriented polypropylene, polyethylene terephthalate, and aluminum foil. Binder addition in finished ink ranges from 4 wt% to 10 wt%, with pigment-to-binder ratios between 0.8:1 and 2.0:1 depending on pigment oil absorption and dispersion demand. Ink concentrates are dispersed on a high-speed dissolver or bead mill to a Hegman grind of 5–7, then reduced to press viscosity of 18–25 s on a Zahn cup #2 before loading onto flexographic presses with 600–800 LPI anilox rolls or gravure cylinders with 50–70 μm cell depth. PVB WW-A-10 provides adhesion to metallized film and contributes to lamination bond strength after adhesive application; bond strength is measured per ASTM F904 or ASTM D1876 after 24 h curing. The main processing constraint is resolubility: PVB resins with low hydroxyl content dissolve slowly in alcohol-rich solvents, and higher-molecular-weight fractions can dry on plate cylinders and cause pinholing, so solvent blends are modified with 2–5 wt% propylene glycol monomethyl ether acetate or ethyl lactate to extend open time. For food-contact printed laminates, the binder must be evaluated under 21 CFR 175.300 and EU Regulation 10/2011 migration testing with the intended food simulant; because published data for PVB WW-A-10 under all food simulants is limited, end-use compliance must be confirmed by the converter using the final laminate structure.

    When PVB WW-A-10 Replaces Ethyl Cellulose in Low-Temperature Thick-Film Pastes

    PVB WW-A-10 is evaluated as a binder and rheology modifier in thick-film conductor and resistor pastes when curing temperatures below 200 °C are required for polymer film substrates or glass components that cannot tolerate ethyl cellulose burnout schedules. Replacement of ethyl cellulose with PVB WW-A-10 alters screen-printing rheology: cone-plate apparent viscosity at 10 s⁻¹ may range from 15 Pa·s to 45 Pa·s depending on silver flake surface area, solvent blend, and binder concentration. The paste is processed through a three-roll mill at 30–40 °C roll temperature, printed through 230–325 mesh stainless steel screens with 15–25 μm emulsion thickness, dried at 80–120 °C, and cured in a forced-air oven at 150–180 °C for 30–60 min. PVB-based pastes offer shorter drying cycles and lower carbon residue than ethyl cellulose at these temperatures, but residual hydroxyl content increases moisture sensitivity and may lead to screen drying during extended print runs. Adhesion after thermal cycling is measured per ASTM D3359, and electrical line resistance is evaluated per IPC-TM-650 method 2.4.1; screen-print slump is assessed by printing a 200 μm line and measuring width change after 5 min in a 25 °C, 50% RH environment. Because published data for PVB WW-A-10 in thick-film pastes is limited, formulation trials require factorial variation of binder-to-solids ratio and solvent evaporation rate to establish lot-specific printability and slump resistance before production release.

    As a heat-sealable coating for aluminum foil lidding, PVB WW-A-10 is applied from an ethanol/methyl ethyl ketone solution at 3–6 g/m² dry coat weight and heat-sealed to polystyrene or polyvinyl chloride cups at 160–190 °C, 0.3–0.6 MPa, and 1–2 s dwell; seal strength is tested per ASTM F88. The main processing constraint is moisture pickup above 60% RH, which reduces seal tack and requires pre-drying of the coated web at 60 °C for 30 s before sealing.

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    Certification & Compliance
    More Introduction

    Polyvinyl butyral grade PVB WW-A-10 is supplied as a water-white thermoplastic resin and film-forming grade for laminated safety-glass interlayers, optical bonding sheets, and coating-binder systems requiring low haze and regulated adhesion to glass. The designation places the product within the poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) family; because no complete public datasheet for the exact WW-A-10 grade is available, the numerical ranges presented below refer to the low-colour PVB class into which the product falls and are not certified replacements for supplier specifications. Typical low-colour PVB resin contains 17–23 wt% vinyl alcohol residue, 0–2.5 wt% vinyl acetate residue, and 75–83 wt% butyral units, with a neat-resin glass transition temperature between 70 °C and 80 °C. The product is normally soluble in ethanol, methanol, 2-propanol, tetrahydrofuran, and solvent mixtures based on toluene plus n-butanol, while it disperses or swells in water; the Hansen solubility parameters of PVB are commonly reported in the 9.1–9.5 (cal/cm³)^0.5 total solubility-parameter range, which is used to select solvent blends for cast-film and high-solids coating formulations.

    What Optical and Moisture Specifications Apply to Low-Colour PVB Film?

    For safety-glass interlayer applications, low-colour PVB film is specified by luminous transmittance, haze, yellowness index, and residual moisture content. Laminated-glass processors should verify WW-A-10 film against ISO 12543-2 and ASTM D1003-21; a typical water-white PVB interlayer at 0.76 mm thickness exhibits luminous transmittance above 85%, haze below 2%, and yellowness index below 1.5 under D65 illumination and a 10° observer. Residual moisture in the interlayer is a process-critical variable because excess water at the glass interface during autoclave cycles produces edge clouding and a measurable reduction in adhesion. Commercial PVB film is conditioned to 0.35–0.55 wt% moisture before lamination; climate-controlled layup rooms are maintained at 20–25 °C and 20–30% RH. Before extrusion, the incoming resin should be dried to below 0.2 wt% moisture to prevent bubble formation at melt temperatures above 190 °C. For finished film, adhesion to glass is controlled primarily by residual vinyl alcohol content and plasticizer package rather than by surface energy alone.

    Beneath the laminating surface-performance envelope, melt rheology controls extrusion and film-converting behaviour. Plasticized PVB exhibits shear-thinning with a power-law index commonly between 0.2 and 0.4 in the 100–1000 s⁻¹ shear-rate window at 150–200 °C. Typical cast-film lines use a single-screw extruder with an L/D ratio of 30:1 to 44:1, a barrier screw, and a coat-hanger die with lip gap 0.5–1.2 mm; barrel set points range from 130 °C to 200 °C, while die zones are held at 175–210 °C. Melt pressure at the breaker plate is generally 80–150 bar, depending on throughput and plasticizer concentration. Published data for WW-A-10 under these exact conditions are limited; the window is derived from PVB grades of similar hydroxyl content and solution viscosity. Capillary rheometry according to ISO 11443:2021 should be used to screen shear viscosity before specifying screw speed, because residual acetate and PVOH content can shift shear viscosity by 20–30% between nominally similar PVB grades.

    Plasticizer Compatibility and Adhesion Control in the WW-A-10 Grade

    When plasticized PVB is formulated for laminated-glass interlayers, triethylene glycol di-2-ethylhexanoate and dibutyl sebacate are the principal external plasticizers. Their compatibility with PVB depends on the vinyl alcohol residue and the butyral-to-acetate ratio. Typical plasticizer loading for PVB film falls between 20 phr and 40 phr; higher loadings increase elongation and reduce tensile modulus. At 30 phr triethylene glycol di-2-ethylhexanoate, plasticized PVB film typically shows tensile strength in the 20–28 MPa range and elongation at break above 200% under ASTM D638-14, but these values are class-typical and not certified for WW-A-10 without supplier data. Glass adhesion is evaluated as pummel value on a 0–10 scale on 300 mm × 300 mm laminates after controlled fracture at −20 °C; adhesion generally decreases with higher plasticizer concentration and increases with residual vinyl alcohol content. PVB grades containing 18–21 wt% vinyl alcohol provide strong adhesion for automotive windshield builds, while lower-hydroxyl grades may be selected where reduced glass adhesion is required. Differences from ionoplast interlayers are quantitative: ionoplast sheet typically displays shear moduli above 100 MPa at 25 °C, whereas plasticized PVB is time-temperature dependent with shear modulus commonly in the 0.5–5 MPa range at 25 °C and 1 Hz. Therefore WW-A-10 is specified where soft-interlayer impact energy absorption and acoustic damping are required, not where high post-breakage stiffness and long-term shear transfer are governing design criteria.

    Table 1. Representative transparent interlayer property ranges; values are class-typical and not grade-specific certified data for PVB WW-A-10.
    Property / test methodPVB low-colour classEVA interlayerIonoplast sheet
    Density, ISO 1183-1:20191.07–1.10 g/cm³0.95–0.97 g/cm³0.95–0.96 g/cm³
    Tensile strength at break, ASTM D638-1420–28 MPa15–25 MPa34–45 MPa
    Elongation at break, ASTM D638-14200–300%300–500%400–500%
    Storage shear modulus at 25 °C, 1 Hz, ISO 6721-60.5–5 MPa2–20 MPa100–300 MPa
    Yellowness index, ASTM E313-20< 1.5< 2.0< 2.0
    Equilibrium moisture at 50% RH, ISO 62:20080.4–0.6 wt%0.1–0.2 wt%0.0–0.1 wt%

    Regulatory compliance for PVB WW-A-10 in laminated glass and coating applications is established through end-product standards rather than as an independent resin specification. For automotive glazing, laminated glass must meet ECE R43, ANSI/SAE Z26.1, or GB 9656; these are impact, optical, and adhesion tests on the complete glazing, and the interlayer is not certified in isolation. For architectural glazing, the ISO 12543 series and EN 14449 define laminated glass and laminated safety glass performance, while ASTM E313-20 is used for yellowness index. Material safety and sustainability statements should be obtained from the supplier as REACH registration and Directive 2011/65/EU certificates; heavy-metal and residual monomer limits are batch-specific. Storage of PVB resin and film should be maintained below 35 °C and below 60% RH; opened containers should be re-sealed under dry nitrogen if storage exceeds 72 h.

    In solvent-borne coating and wash-primer systems, PVB WW-A-10 serves as a film-forming binder with adhesion to steel, aluminum, and glass. Typical wash-primer formulations use PVB at 5–12 wt% of the liquid coating with phosphoric acid and zinc chromate or zinc phosphate as active pigments; the PVB binder provides dry-film thickness and adhesion without acting as a crosslinker. Solvent blends based on methyl ethyl ketone, toluene, and n-butanol are used to dissolve the resin while maintaining total solubility parameter near 9.2 (cal/cm³)^0.5. Coatings formulated with PVB WW-A-10 should be filtered through a 10–25 µm absolute filter to remove microgel and undispersed stabilizer residues. Published data for WW-A-10 in exact wash-primer formulations are limited; batch-to-batch variation in residual hydroxyl content can shift acid etch adhesion on aluminum by more than 1 grade on a 0–5 crosshatch scale under ISO 2409.

    Ceramic tape-casting binders based on PVB WW-A-10 may be specified if the supplier certifies low ash content and low alkali metal levels. Tape-casting formulations typically combine PVB binder at 4–9 wt% of the slurry with a plasticizer-to-binder ratio of 0.5:1 to 1:1, a solvent blend, and a defoamer; green tape then undergoes debinding at 350–450 °C in air. The residual ash after debinding must be verified for the WW-A-10 lot because sodium and calcium residues above 500 ppm can alter the dielectric properties of the sintered ceramic. This application is highly sensitive to batch-to-batch viscosity, and a rotational viscometer reading at 20 °C on a 10 wt% resin solution should be requested from the supplier.

    Film blocking and roll-release behaviour in PVB WW-A-10 are controlled by surface roughness, plasticizer migration, and storage temperature. For interlayer rolls stored at 25–35 °C, blocking can become irreversible if compressive stress exceeds 50 kPa for more than 24 h; palletized rolls should be stored vertically and never stacked more than two high. A chilled cast-roll temperature of 12–18 °C on the film line produces a matte surface with average roughness Ra between 0.5 µm and 2.0 µm, which is critical for de-airing in the layup. If surface roughness is too low, air channels collapse during vacuum bagging and edge bubbles form in the autoclave.

    How Does WW-A-10 Differ from Higher-Hydroxyl or Higher-Molecular-Weight PVB Resins?

    Within the PVB family, product differentiation is driven by three resin variables: residual polyvinyl alcohol content, molecular weight, and plasticizer acceptance. The WW-A-10 designation is most consistent with a low-colour, medium-hydroxyl grade, but the absence of a public datasheet means that exact molecular weight and moisture-equilibrium values remain unverified. Higher-PVOH grades in the 20–23 wt% range typically raise glass adhesion, increase moisture absorption, and require stricter pre-drying. Lower-PVOH grades in the 11–16 wt% range can reduce melt viscosity and improve solvency but may exhibit lower tensile strength after plasticization. Molecular weight, often expressed as solution viscosity in 10% ethanol solution or as melt volume-flow rate under ISO 1133-1:2022, controls processability: a low-viscosity PVB may flow at melt temperatures 20–30 °C below a high-viscosity grade, reducing die pressure and improving wet-out on glass. For WW-A-10, the expected advantage in transparent lamination is optical neutrality and consistent adhesion, but published data for this specific configuration is limited. Compared with coextruded trilayer acoustic PVB stacks, a monolayer WW-A-10 film offers simpler die construction and lower edge-trim scrap but may not match the broadband acoustic loss factor of multilayer systems with a plasticizer-rich core layer.

    When Laminated-Glass Autoclave Conditions Must Be Adjusted

    The autoclave cycle for PVB WW-A-10 laminated glass is governed by residual air solubility, plasticizer volatility, and the glass-surface reaction. Standard PVB lamination uses a pre-pressing nip roll or vacuum bag stage followed by autoclave exposure at 120–140 °C and 10–14 bar for 45–90 min in air. Cooling should not proceed faster than 0.3 °C/min until the panel is below 60 °C to avoid edge stresses and optical distortion. If WW-A-10 contains a lower plasticizer concentration than a standard automotive grade, adhesion may require more time at temperature; if it contains a higher plasticizer concentration, edge adhesion may be reduced and the pummel value should be checked on a production-run sample. Layup rooms for PVB are normally held at 20–25 °C and 20–30% RH; excursions above 30% RH during glass stacking can produce edge clouding and require longer autoclave time to remove dissolved water. The final adhesion should be verified by compressive shear testing on a laminated-glass coupon according to a recognized method, rather than by visual inspection alone.

    PVB WW-A-10 should not be compounded with amine-based additives or isocyanates unless formulation-specific trials demonstrate stability, because free amines can accelerate hydrolysis of the butyral ring and reduce film toughness. Avoid combining PVB with strong alkaline aqueous media above pH 9 during processing, as hydrolysis of the vinyl acetate and vinyl alcohol segments can occur. The resin is also incompatible with non-polar aliphatic hydrocarbons and with many ketone-free aliphatic solvents; solvent selection should remain in the polar and hydrogen-bonding regions defined by Hansen solubility parameters. If pre-drying is performed at temperatures above 85 °C, resin blocking and yellowing can increase; therefore dryers with dew-point-controlled air and low airflow channeling are preferred.