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Anhui Liwei Chemical Co., Limited.

Wanwei PVA 17-95(L) (PVA 095-27)

    • Product Name: Wanwei PVA 17-95(L) (PVA 095-27)
    • 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 895963
    Chemical Formula (C2H4O)n
    Cas Number 9002-89-5
    Appearance white granular powder
    Average Degree Of Polymerization 1700
    Degree Of Hydrolysis 95.0 mol%
    Viscosity 4 Percent Aqueous Solution 20c 27.0 mPa·s
    Ph 4 Percent Aqueous Solution 6.0-7.0
    Volatile Content ≤5.0 wt%
    Ash Content ≤0.5 wt%
    Melting Point 180-220 °C
    Density 1.25-1.31 g/cm³
    Solubility soluble in hot water; insoluble in common organic solvents
    Molecular Weight approximately 74,800 g/mol

    As an accredited Wanwei PVA 17-95(L) (PVA 095-27) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Wanwei PVA 17-95(L) (PVA 095-27) is supplied in 25 kg multi-walled paper bags with an inner plastic liner.
    Container Loading (20′ FCL) 20′ FCL loading of Wanwei PVA 17-95(L): palletized bags securely stowed in a clean, dry 20-foot container, protected from moisture and direct heat.
    Shipping Wanwei PVA 17-95(L) ships as a white granular solid in sealed multi-layer paper bags or woven bags with PE liner. Keep dry, avoid moisture and dust accumulation, store in cool, ventilated area. Non-hazardous under normal conditions; handle with care to prevent bag damage.
    Storage Store Wanwei PVA 17-95(L) in a cool, dry, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep the original container tightly sealed to prevent moisture absorption and contamination. Avoid generating dust. Ensure compatibility with surrounding materials; keep separate from oxidizing agents and acids. Use within recommended shelf life, typically up to two years.
    Shelf Life Shelf life is typically 12 months from manufacture when stored in original sealed packaging in a cool, dry place.
    Application of Wanwei PVA 17-95(L) (PVA 095-27)
    On high-speed air-jet and rapier looms running in excess of 800 weft insertions per minute, warp yarns of combed cotton, polyester/cotton blends, and viscose are subjected to cyclic abrasion, tension surges exceeding 30 cN/tex, and frictional heating that rapidly erode unsized staple-fibre assemblies. Wanwei PVA 17-95(L)—with a 4% aqueous solution viscosity of 17–22 mPa·s (ISO 307, Brookfield LV, spindle 1, 60 rpm) and a degree of hydrolysis of 95.0–96.0 mol%—develops a cohesive, elastic film that penetrates yarn interstices while forming a tough surface sleeve. The low-ash variant (sulfated ash typically ≤0.3 wt% according to ISO 3451-1) prevents abrasive deposit build-up on reed, heald eyes, and drop wires; in comparative mill trials on Sulzer projectile machines operating at 320–380 rpm, warp break frequency was reduced by an estimated 25–40% relative to a standard-ash PVA of equivalent viscosity. The size box must hold a nipping pressure of 15–25 kN/m at the squeeze rolls and a bath temperature of 80±3°C to forestall skin formation, a known failure mode for partially hydrolysed PVAs when the surface temperature drops below 75°C or circulation stagnates. A non-silicone defoamer dosed at 0.05–0.2 wt% on size solids is often necessary to suppress foam generated by the acetate-group surface activity in high-shear pumping circuits. Desizing is carried out in a multi-box washing range at 92–95°C with an oxidative additive such as hydrogen peroxide (2–4 mL/L of 35% H₂O₂) or sodium persulfate; complete size removal is confirmed by iodine spot test. The BOD₅ contribution of the PVA size is approximately 0.03–0.05 kg O₂/kg in acclimated activated sludge, substantially lower than that of starch-based sizes, facilitating compliance with textile effluent consent limits under IUWWT Directive (91/271/EEC) derivative local permits. Film tensile strength measured per ASTM D882 at 23°C, 50% RH and 500 mm/min crosshead speed is roughly 38–52 MPa with elongation at break of 140–200%, and the refractive index of 1.52 matches that of cellulose, making the sized yarn transparent to optical quality-inspection systems such as Uster Quantum clearers.
    Property (film cast from 7% solution, dried 105°C, conditioned 23°C/50% RH)PVA 17-95(L)Oxidized corn starchSodium CMC
    Viscosity stability (retention after 8 h at 85°C, ISO 2555)>95%40–65% (retrogradation)70–85%
    Elongation at break (ASTM D882)180±20%4–6%20–30%
    Abrasion resistance (Taber cycles, CS-10 wheels, 500 g load, to failure)>50 0008 000–12 00015 000–25 000
    Desizing completeness (iodine test after 5 min wash at 95°C, 0.5% NaOH)No blue stainFaint residual stainModerate stain

    How Does Low-Ash PVA Reduce Calender Contamination in Surface Sizing?

    Modern film-press and metered-size-press units on fine paper machines operating at webs speeds above 1200 m/min encounter recurring calender deposit problems when conventional PVA grades carry soluble mineral residues. Wanwei 17-95(L) with sulfated ash ≤0.3% (ISO 3451-1) supplies only minimal calcium, sodium, and silicon ions to the size-press recirculation loop, thereby suppressing the formation of hard, tacky deposits on the heated calender rolls that would otherwise require machine stoppage for cleaning as frequently as every 6–8 hours. Industrial case reports indicate that switching from a standard-ash 17-95 to the “L” grade can extend cleaning intervals by a factor of 2–3, with direct maintenance-cost savings and fewer web breaks during calender threading. The PVA is applied as a 3–8 wt% aqueous solution at a typical dry pick-up of 1.0–2.5 g/m² per side, often in combination with an optical brightening agent and a small amount of a non-ionic surfactant to improve wetting on internally sized base paper. ISO 535 (Cobb60) water absorption values respond steeply to increasing PVA coverage, as shown in the table below for a wood-free 80 g/m² sheet. The low-ash chemistry also preserves the fluorescence quantum yield of stilbene-based optical brighteners because transition metal ions that quench OBA emission are practically absent. Formulation must respect charge-incompatibility boundaries: co-addition of strongly cationic wet-end additives such as poly-DADMAC or high-charge-density polyamines can induce associative phase separation in the size-press bath, forming gummy precipitates that block metering rods and score the applicator roll. Compliance with BfR Recommendation XXXVI for paper and board intended for food contact is achievable when the PVA is the sole film former and residual vinyl acetate monomer is <5 ppm as determined by headspace GC-MS per EN 13628-2.
    PVA pick-up (g/m² per side)Cobb60 (g/m²) – ISO 535IGT dry pick (cm/s) – ISO 3783
    0 (base paper)50±380±10
    0.535±2150±15
    1.025±2210±20
    1.518±1.5260±20
    2.015±1290±25
    Remoistenable gummed tapes and peel-and-stick envelope closures demand a film former that rehydrates rapidly under a damp fingertip while offering adequate dry-blocking resistance during storage in high-humidity distribution environments. The 17-95(L) grade is dissolved at 18–22 wt% solids in a heated jacketed vessel equipped with a low-shear anchor agitator, together with glycerol (5–12 phr on PVA weight) as a plasticising humectant and, optionally, 0.5–2 phr of sorbitol to fine-tune the moisture-retention profile. The adhesive is applied by reverse-roll or slot-die coating onto kraft paper, glassine, or filmic release liners at a wet-film thickness of 50–100 µm, then dried through a three-zone forced-air convection tunnel with temperature settings of 80°C, 105°C, and 110°C to a final moisture content of 6–9%. The low-ash purity (ash ≤0.3%) is critical for maintaining optical clarity of the dried adhesive layer and for preventing die-lip build-up that can generate longitudinal striations. Remoistening speed is defined as the time needed for the film to develop a 180° peel force of ≥2 N/25 mm (ASTM D903, 0.5 s dwell) after a single moistening stroke; formulations based on 17-95(L) typically achieve this threshold in under 1.0 s when conditioned at 50% RH. At relative humidity sustained above 80%, however, the PVA network plasticises sufficiently to trigger blocking. Incorporation of 1–3 phr of a synthetic styrene-acrylic latex improves room-temperature blocking resistance but inevitably extends remoistening time; the formulator must balance these properties for the intended climatic exposure envelope. Calcium chloride or other polyvalent metal salts, occasionally proposed as hygroscopic tackifiers, are categorically incompatible—the instantaneous formation of a gelatinous PVA–metal complex precipitates irreversibly and will permanently plug coating heads and fine distribution lines.

    Emulsion Polymerization Protective Colloid: Bridging Water Resistance and Colloidal Stability

    A semi-batch emulsion polymerization of vinyl acetate homopolymer or vinyl acetate–butyl acrylate copolymer intended for wood assembly adhesives can exploit PVA 17-95(L) as the primary protective colloid, typically charged at 1.5–3.0 wt% on total monomer together with a co-stabilising anionic surfactant such as sodium lauryl sulfate at 0.3–0.8 wt%. The reactor is initially loaded with a 10–15% fraction of the monomer and the full PVA solution, then heated to 72±2°C under a nitrogen blanket. Initiation with potassium persulfate (0.2–0.4 wt% on monomer, added as a 5% aqueous solution) triggers a seed stage, after which the remaining monomer and a parallel initiator stream are fed over 3–4 hours. The 95% hydrolysis character reduces the cold-water solubility of the PVA graft shell compared with 88% hydrolysis grades, yielding an adhesive film with measurably higher wet cohesion yet a narrower colloidal stability window. If the exotherm—approximately 1050 kJ/kg of vinyl acetate—exceeds jacket cooling capacity and the batch temperature climbs above 76°C, particle aggregation proceeds rapidly and the emulsion can undergo catastrophic shock-coagulation within minutes. When the process is correctly maintained, the final latex exhibits a Brookfield viscosity (ISO 2555, LV, spindle 4, 12 rpm) of 15 000–40 000 mPa·s at 50–55% solids content and a z-average particle size of 400–800 nm (ISO 22412, dynamic light scattering). The adhesive produced by compounding the emulsion with a plasticiser, filler, and a preservative is capable of satisfying durability class D2 per EN 204:2016: after assembling beech lap joints and a 7-day conditioning cycle, the shear strength following 4 hours water immersion at 23°C must surpass the minimum required value specified in clause 5.2 of the standard, a demand consistently met by PVA 17-95(L)-stabilised systems when the resin-to-filler ratio is appropriately adjusted. However, the same adhesive will outright fail the more aggressive D3 test (immersion in water at 60°C or boiling-water test) because the protective colloid re-disperses, making the grade unsuitable for load-bearing exterior joinery. Pre-drying of the PVA powder before use is strongly advised at ambient humidity above 60% RH, as the partially hydrolysed structure absorbs moisture rapidly; otherwise, lump formation and variable dissolution rates compromise batch-to-batch emulsion consistency.

    When PVA 17-95(L) Serves as a Sacrificial Interleaf in Automotive Lamination

    Before the bending and autoclave lamination of laminated safety glass, individual glass plies are separated by a temporary, washable coating that prevents surface scratches during handling and aids vacuum hold-down on robotic grippers. A 5–8 wt% aqueous solution of Wanwei 17-95(L), containing 0.3–0.5% of a wetting agent such as 2-butoxyethanol to achieve a surface tension below 40 mN/m, is applied to the cleaned glass by a #8–#14 Meyer rod and force-dried with infrared radiation to a dry film thickness of 8–15 µm. The coating must exhibit a peel adhesion to float glass in the range 0.3–1.0 N/25 mm when measured according to ASTM D3330 (Method A, 180° peel at 300 mm/min)—enough to resist delamination during transport yet weak enough to permit clean removal without residue. After assembly with a polyvinyl butyral interlayer and autoclave bonding, the sacrificial interleaf is dissolved by a 30–35°C water spray containing a mild non-ionic detergent; dissolution time for a 10 µm dry film at 30°C in still water is characteristically under 120 seconds, with the low-ash grade leaving no detectable mineral haze in the final laminate when inspected under polarised light per ASTM C1036. Operating outside this thermal range causes control problems: below 25°C the dissolution rate slows prohibitively, while above 45°C the plasticised PVA film can soften and smudge, transferring residue onto adjacent glass surfaces. A critical incompatibility exists with glass pre-treated with amino-functional silane coupling agents; these react with PVA hydroxyls to form a crosslinked interphase that resists water wash-off and demands aggressive mechanical scrubbing, ultimately defeating the purpose of the sacrificial layer.
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    Certification & Compliance
    More Introduction

    Anhui Wanwei Group designates this partially hydrolysed polyvinyl alcohol as PVA 17-95(L), alternatively coded PVA 095-27. It occupies the intermediate alcoholysis window between fully saponified homopolymers and the highly water-sensitive 88 mol% grades, with a nominal degree of polymerisation of 1700 and a hydrolysis degree controlled to 95.0 ± 1.0 mol%. The “L” suffix denotes a low-methanol-extraction post-treatment, resulting in reduced residual vinyl acetate monomer and an ash ceiling of 0.2%, which distinguishes this grade from standard 17-95 material in applications where ionic contamination compromises dielectric performance or adhesive bond stability. Film cast from 4% aqueous solution exhibits tensile strength at break in the range 40–50 MPa (GB/T 1040.3, conditioning at 23 °C, 50% RH) with elongation at break 250–350%, reflecting the balance between amorphous domain mobility and residual crystalline anchoring contributed by retained acetate groups.

    Specifications and Analytical Compliance Matrix

    Parameter Method Typical Value
    Viscosity, 4% aqueous solution at 20 °C GB/T 12010.2–2010 (Brookfield LV, spindle 1, 60 rpm) 24–32 mPa·s
    Alcoholysis degree GB/T 12010.7–2010 (alkaline saponification titration) 94.5–96.0 mol%
    Volatile matter GB/T 12010.4–2010 (105 °C, 3 h) 5.0%
    Ash (as Na₂O) GB/T 12010.5–2010 (700 °C ignition) 0.2%
    pH GB/T 12010.8–2010 (4% solution) 5.0–7.0
    Bulk density ISO 60:1977 0.40–0.55 g/cm³
    Particle size (retained on 40 mesh) GB/T 6003.1–2012 2.0%

    What Differentiates a 95 mol% Hydrolysed PVA from Fully Saponified and Low-Hydrolysis Grades?

    Fully saponified grades such as 17-99 (hydrolysis ≥ 98.5 mol%) require dissolution temperatures above 90 °C and yield films with minimal cold-water sensitivity and tensile modulus exceeding 4.5 GPa. At the opposite end, 17-88 (88 mol%) dissolves readily in water at 10–15 °C but exhibits high surface tack and tensile strength below 30 MPa. The 95 mol% structure in 17-95(L) balances solubility onset at 40–50 °C with a storage modulus G’ plateau in the semi-dilute regime approximately 2.3 kPa (6% solution, 25 °C, oscillatory frequency 1 Hz), providing sufficient chain entanglement for cohesive film formation without the severe crystallinity-driven brittleness observed in fully hydrolysed analogues. Residual acetate groups reduce hydrogen-bond-driven ordering, preserving ductility under cyclic loading relevant to flexographic plate mounting tapes and repulpable splicing adhesives.

    In textile warp sizing lines operating at slasher speeds above 80 m/min, the size liquor composed of 6–8% PVA 17-95(L), 3% acrylic copolymer, and 0.8% tallow wax is maintained at 85–88 °C in a Sucker Müller SMR size box. Delivered add-on on Ne 30 ring-spun cotton warp is 10–12% dry weight. If box temperature drops below 80 °C, surface skinning on the immersion rolls produces gel specks that deposit within the reed dents, causing warp-end abrasion on air-jet looms operating at 900 picks/min. Film abrasion resistance, measured by Zweigle G55 Gauge with 400-cycles under 50 g load, shows a mass loss ≤ 2.5 mg for films cast from liquors conditioned at 88 °C. Migration of the size film during quiescent storage in weaving sheds where humidity exceeds 85% RH leads to blocking; pre-drying warp sheets to 6–8% moisture content before lease separation is mandatory.

    When 17-95(L) Replaces Higher-Viscosity Grades in Emulsion Polymerisation Protective Colloids

    In the suspension polymerisation of vinyl acetate monomer initiated by azobisisobutyronitrile (AIBN) at 0.05% on monomer, PVA 17-95(L) is dosed at 1.2–1.8% (w/w monomer) into the aqueous phase. The low ash content minimises interference with the free-radical initiation sequence, while the narrow hydrolysis distribution reduces polydispersity-driven partitioning effects that would otherwise widen the particle size distribution. Post-polymerisation analysis by laser diffraction (ISO 22498) confirms a volume median diameter Dv50 of 80–120 µm when the agitation is set to produce a tip speed of 3.5 m/s in a 3 m³ glass-lined reactor with a Pfaudler retreat-blade impeller. Substitution of a 17-99 grade under identical conditions raises Dv50 to 180–240 µm and increases coarse fraction (>500 µm) due to poor interfacial tension reduction, while 17-88 over-stabilises the dispersion and generates excessive fines (Dv50 < 20 µm) that raise emulsion viscosity beyond pumpable limits.

    Processing Temperature Limits and Degradation Kinetics in Twin-Screw Extrusion

    Compounding PVA 17-95(L) with glycerol (15 phr), urea (8 phr), and stearamide (0.5 phr) for water-soluble blown film requires a co-rotating twin-screw extruder with L/D = 40:1 and a modular screw profile incorporating two kneading blocks of 45° stagger angle followed by a reverse-flighted intensive mixing zone. Barrel temperature profile: Zone 1 90 °C, Zone 2 130 °C, Zone 3 155 °C, Zone 4 165 °C, die adapter 170 °C. Plasticising must be complete before Zone 2; residual crystalline domains entering Zone 3 create viscosity heterogeneities that manifest as ±15% thickness variation in the final film (ASTM D6988). Degradation onset detected by DSC at 200 °C (ramp 10 K/min, nitrogen purge) produces acetic acid, which autocatalytically accelerates chain scission. Residence time is therefore restricted to < 120 s, monitored by a graphite tracer pulse. Pre-drying of the powder in a desiccant hopper dryer at 80 °C for 4 h until residual moisture is < 0.5% is mandatory; otherwise, steam devolatilisation at the vent port creates bubble defects and reduces film dart impact by 40–50% (ISO 7765-1). Purging with linear low-density polyethylene at shift end prevents carbonised deposits at the die lips.

    In low-solids oilfield fluid loss pills, 0.8% PVA 17-95(L) is hydrated in 2% KCl brine, after which controlled crosslinking with sodium tetraborate decahydrate at 0.015% generates a shear-reversible gel. Gel time at 25 °C is 18 min, reaching an equilibrium storage modulus G’ of 420 Pa (vane rheometer, stress 5 Pa). Concentrations exceeding 0.03% borax produce syneresis within 6 hours static aging at 80 °C, rendering the pill ineffective for loss zone sealing. This system is incompatible with amine-based shale inhibitors; pH drift above 8.2 deacetylates the polymer backbone, shifting cloud point and collapsing the gel network.

    Comparative Profiles of Selected Wanwei Polyvinyl Alcohol Grades

    Grade Designation Degree of Polymerisation Hydrolysis (mol%) Viscosity 4%, 20 °C (mPa·s) Ash (%) Key Differentiation
    05-88 500 88 ± 1 5–7 0.5 Ultra-low viscosity; cold water soluble; used in paper coating pigment binders.
    17-88 1700 88 ± 1 21–27 0.5 High tack; cold water soluble; mainstay for remoistenable adhesives.
    17-95(L) 1700 95 ± 1 24–32 0.2 Low ash, controlled warm-water solubility; engineered for electronic-grade adhesives and emulsion stabilisation.
    17-99 1700 ≥ 98.5 26–34 0.5 Hot-water soluble; maximum tensile strength; used in polarising film and PVB interlayer.
    20-99 2000 ≥ 98.5 34–42 0.5 Highest viscosity fully hydrolysed grade; superior film toughness.

    For a simple repulpable bookbinding adhesive, PVA 17-95(L) is dissolved at 12% solids in water heated to 60 °C and blended with acid-modified corn starch in a 1:1.2 ratio.