| HS Code | 716992 |
| Product Name | SELVOL Polyvinyl Alcohol 165 |
| Chemical Name | Poly(vinyl alcohol) |
| Cas Number | 9002-89-5 |
| Appearance | White to cream granular powder |
| Hydrolysis Degree | 99.3 - 100 mole% |
| Viscosity | 62 - 72 mPa·s (4% aqueous solution at 20°C) |
| Ph | 5.5 - 7.5 (aqueous solution) |
| Ash Content | ≤ 1.2% |
| Volatile Matter | ≤ 5.0% |
| Solubility | Soluble in hot water; practically insoluble in cold water |
| Melting Point | Approximately 230°C |
| Density | Approximately 1.25 - 1.35 g/cm³ |
As an accredited SELVOL Polyvinyl Alcohol 165 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | SELVOL Polyvinyl Alcohol 165 is supplied as a white powder in 25 kg multi-layer paper bags with polyethylene liner. |
| Container Loading (20′ FCL) | SELVOL Polyvinyl Alcohol 165 is loaded in a 20′ FCL on pallets, securely stowed and protected from moisture. |
| Shipping | SELVOL Polyvinyl Alcohol 165 ships as a dry, water-soluble powder in lined bags or drums. Keep containers sealed and protected from moisture, humidity, and direct sunlight. Avoid dust-generating conditions and store in a cool, well-ventilated area. Not classified as hazardous, but practice good housekeeping to prevent slips and dust accumulation. |
| Storage | Store SELVOL Polyvinyl Alcohol 165 in a cool, dry, well-ventilated area, keeping containers tightly sealed when not in use. Protect from moisture, humidity, and direct sunlight, as wet material can cause handling issues. Keep away from heat, flames, and oxidizing agents. Avoid generating dust; maintain good housekeeping to reduce static ignition risk. |
| Shelf Life | Shelf life is typically 2 years when stored in a cool, dry area with original container tightly sealed. |
Selvol Polyvinyl Alcohol 165 is a partially hydrolyzed polyvinyl alcohol grade supplied in solid granular form. Incoming material is typically qualified against a certificate of analysis that reports a 4% aqueous solution viscosity of 5.2–6.2 cP at 20 °C, a hydrolysis range of 87.0–89.0 mol%, an ash content not exceeding 0.5 wt%, and a volatile content below 5.0 wt%. For method alignment, viscosity characterization follows ISO 15023-2:2019 with a Brookfield LV rotational viscometer, spindle LV-1, at 60 rpm after complete dissolution at 85 °C for 30 min and cooling to 20 °C. The grade’s intermediate molecular weight and partial hydrolysis position it in applications where surface activity, film flexibility, and cold-water solubility are required without the gel-temperature limitations of highly hydrolyzed grades.
Before aqueous dissolution, the granulate should be stored at relative humidity below 60%; if exposed to higher humidity, surface moisture can exceed 5 wt% and reduce discharge from loss-in-weight feeders. Pre-drying at 40–50 °C in a desiccant dryer for 2–4 h is used where hopper bridging has been observed on production lines. The material is incompatible with borate ions, which cause rapid gelation in solution unless controlled crosslinking is intended. Dissolution must not be carried out at temperatures above 95 °C in high-shear mixers, because localized heating can form insoluble skins on the granule surface.
| Downstream sector | Regulatory anchor | Principal test method |
|---|---|---|
| Paperboard adhesive | FDA 21 CFR 175.105 | ASTM D1876-08(2015) |
| Emulsion polymerization | FDA 21 CFR 176.170 | ISO 2555:2018 |
| Paper coating | FDA 21 CFR 176.180 | TAPPI T 441 |
| Textile warp sizing | ZDHC MRSL V3.1 | ISO 6060:1989 |
| Ceramic greenware | EU Directive 84/500/EEC | ISO 10545-4:2014 |
| Suspension PVC | EU REACH 1907/2006 | ISO 6401:2022 |
The substitution of dextrin or starch with Selvol 165 in carton-seam adhesives changes low-shear viscosity only when the aqueous solution is prepared within a defined thermal window. A typical preparation sequence charges cold water at 20–25 °C into a jacketed mix tank equipped with a low-shear turbine agitator operating at 150–300 rpm; Selvol 165 is sprinkled into the vortex and held in suspension for 10–15 min before steam is introduced. The tank is heated to 85–95 °C and held for 30–45 min to eliminate undissolved microgels. The solution is then cooled to 40–50 °C and blended with plasticizer, filler, and a polyvinyl acetate homopolymer emulsion. In a carton-seam formula, Selvol 165 is typically present at 4–7 wt% of the wet adhesive, with an aqueous stock solution concentration of 10–15 wt%. The adhesive is applied by a roller coater at 25–40 g/m² wet film weight to clay-coated paperboard, followed by compression at a nip pressure of 0.3–0.8 MPa and infrared drying. Batch-to-batch variance on corrugating lines is controlled by measuring the viscosity of the final adhesive at 25 °C with a Brookfield LV viscometer at 20 rpm; the target is typically 1,500–3,500 mPa·s for carton side seams. If viscosity falls below 1,200 mPa·s, adhesive can penetrate the board and cause warp; if viscosity rises above 4,000 mPa·s, transfer from the roller coater becomes non-uniform and starved streaks appear. On high-speed carton gluers running above 300 m/min, the open time of the adhesive is extended by adding plasticizer at 5–10 wt% of the final adhesive. Production equipment includes a jacketed mix tank, a piston pump, and a stainless steel roller coater; the adhesive is recirculated through a 100 µm filter to remove skins formed by evaporation at the trough edge. The terminal products are side-seam cartons, paper tube winding adhesives, and litholaminate gluing. Compliance for food-contact use is anchored to FDA 21 CFR 175.105, and bond performance is monitored by ASTM D1876-08(2015) T-peel testing. Published data for this specific formula configuration is limited, but batch acceptance is based on the comparative data generated under the specified test method.
Pre-dissolved 10 wt% aqueous Selvol 165 is metered into a vinyl acetate-ethylene emulsion reactor at a rate that maintains a monomer-to-protective colloid ratio of 50:1 to 25:1, equivalent to 2–5 wt% protective colloid on total vinyl acetate monomer. The polymerization is run in a jacketed stainless steel reactor with a three-blade retreat-curve impeller at 100–150 rpm, a reaction temperature of 60–80 °C, and an ammonium persulfate initiator feed of 0.2–0.5 wt% on monomer. The partially hydrolyzed grade provides interfacial activity at the monomer-water boundary and produces a shear-thinning emulsion. A known incompatibility occurs when tetraborate ions are introduced before film coalescence; borate ions crosslink the free hydroxyl groups on the polyvinyl alcohol chain and generate a viscosity increase that can destabilize the reactor discharge. Reactor-floor experience shows that deviations in the protective colloid feed rate of more than 10% from the specified ratio during the first 30 min of polymerization produce a measurable shift in final emulsion particle size distribution, which is monitored by laser diffraction using ISO 13320:2020. The finished dispersion is typically filtered through a 150 µm screen to remove coagulum, then used as the base polymer for wood glues, paperboard lamination binders, and nonwoven saturation binders. For nonwoven saturation, the same emulsion is diluted and applied on a padder at 80–120 g/m² wet add-on. The terminal products are PVAc homopolymer wood adhesives, vinyl acetate-ethylene copolymer construction adhesives, and nonwoven textile binders. Food-contact status is determined by the end-use emulsion under FDA 21 CFR 176.170 as a component of paper and paperboard in contact with aqueous and fatty foods, subject to migration testing under 21 CFR 176.170(c). Viscosity acceptance is checked with ISO 2555:2018 at 25 °C; solids content is measured by ASTM D1259. The known operational boundary is the borate incompatibility discussed above; borate ions must be excluded from all reactor feed lines until the emulsion is formulated into the final adhesive and intentional thickening is required.
On high-speed blade coaters, the water retention demand of a coating color containing Selvol 165 is governed less by total binder content than by the interaction between the polyvinyl alcohol chain length and the pH of the pigment slurry. In a typical formulation, Selvol 165 is added as a 10 wt% aqueous solution at 0.5–2.0 parts per 100 parts dry pigment, together with a latex binder at 10–14 parts and calcium carbonate or clay pigment. The coating color is dispersed under high shear in a Cowles disperser at 1,500–3,000 rpm, adjusted to 5–8 wt% total binder solids, and screened through a 100 µm pressure screen before being pumped to the coating head. Application is performed with a bent-blade coater at machine speeds of 800–1,400 m/min; coat weight is maintained at 12–25 g/m² per side. The downstream production process includes infrared drying, air flotation drying, and soft-nip calendering before reel-up. In coated folding carton production, the gloss and smoothness of the final sheet are determined as much by the coater water balance as by subsequent calendering. The formulation containing Selvol 165 is dried in an air flotation dryer with web surface temperature maintained below 105 °C to avoid binder migration. At coating speeds above 1,200 m/min, the high-shear viscosity measured with a capillary viscometer at 10,000 s⁻¹ should remain below 120 mPa·s; above this limit, streaking and blade edge deposits increase. Selvol 165 functions as a co-binder that raises water retention and improves pick strength, but addition above 2.0 parts per 100 parts pigment can produce coating color dilatancy at the blade tip and increase blade deposits on equipment with blade pressures above 1.8 kN/m. The terminal products are coated folding carton stock, label facestock, and coated solid bleached sulphate board. Compliance for direct food contact is addressed through FDA 21 CFR 176.170 and FDA 21 CFR 176.180 for paper and paperboard components. Water absorptiveness is measured by TAPPI T 441; brightness and gloss are measured according to ISO 2470-1:2016 and ISO 8254-2:2016 respectively. For FDA batch release, the coating color is tested for extractives and for total organic carbon under the conditions specified in the applicable regulation. Published data for this specific grade in coating color at machine speeds above 1,400 m/min is limited.
Slasher sizing of polyester/cotton warp yarns at a 7–9 wt% size-box concentration of Selvol 165 produces a dry fiber add-on of 8–10 wt% when squeeze-roll pressure is held at 30–45 N/cm. The size solution is prepared in a high-shear jet cooker at 80–90 °C, transferred to a size box with immersion rolls, and applied to warp sheets at line speeds of 60–120 m/min. The sized yarn passes over drying cylinders maintained at 120–140 °C, then through a lease section and onto a weaver’s beam. Selvol 165 contributes adhesion to hydrophobic polyester surfaces and film flexibility to reduce fiber shedding in the weaving shed. At squeeze pressures below 30 N/cm, pickup can rise above 12 wt%, producing a brittle size film that fragments at the reed; above 45 N/cm, pickup falls below 6 wt% and filament hairiness increases. Desizing is carried out with hot water or oxidative desizing followed by a conventional finishing sequence. The terminal product types are greige woven fabrics for apparel, workwear, and home textiles. Regulatory alignment for textile auxiliaries is managed through the ZDHC MRSL Version 3.1 and, where EU brands are involved, through OEKO-TEX ECO PASSPORT certification of the size formulation. Wastewater COD from PVOH desizing is monitored by ISO 6060:1989; recovery via ultrafiltration is used in mills where discharge consents are below 2,000 mg/L COD.
Dry-pressed ceramic green bodies based on alumina or zirconia formulations exhibit green strength losses if the polyvinyl alcohol binder is plasticized by residual moisture in the spray-dried granulate. Selvol 165 is introduced into the ceramic slurry as a 10 wt% aqueous solution at 0.5–2.0 wt% dry binder on dry ceramic powder, before spray drying. The slurry is atomized in a spray dryer with an inlet temperature of 180–250 °C and an outlet temperature of 80–110 °C, producing free-flowing granules with residual moisture below 1.0 wt%. Production-scale spray dryers used for tile body granulate are typically fitted with rotary atomizers operating at 8,000–12,000 rpm; the granulate median diameter is held between 100–300 µm. The granulate is uniaxially pressed at 40–80 MPa using hydraulic or mechanical presses with tool fill depths set to maintain a compact density of 55–65% of theoretical density. The binder acts as a particle-to-particle film bridging the ceramic grains; its partial hydrolysis and 0.5 wt% maximum ash content minimize localized inorganic residue after burnout. Selvol 165 addition above 2.0 wt% dry solids can increase granule strength but also increase ejection pressure during pressing and produce black core defects during fast firing. Below 0.5 wt%, green strength may fall below 1.0 MPa in three-point bending, increasing breakage during glazing and transport. Thermal removal is conducted in air or nitrogen using a debinding ramp from 25 °C to 550 °C at 0.5–2.0 °C/min, with a dwell at 350–450 °C to complete oxidative degradation before sintering. Terminal products include ceramic tile bodies, technical alumina substrates, and pressed zirconia components. Green strength is measured by three-point bending according to ISO 10545-4:2014 for ceramic tiles or by ASTM C1161-18 for advanced ceramics; dimensional stability is verified by green density measurements using ASTM C20 or equivalent immersion methods. Compliance for ceramic articles intended for plumbing and food-contact use is governed by national ceramic migration limits and, where applicable, EU Directive 84/500/EEC as amended by 2005/31/EC for ceramic articles in contact with food.
In suspension PVC reactors, a partially hydrolyzed PVOH with an intermediate degree of polymerization partitions preferentially at the vinyl chloride-water interface and reduces coalescence of monomer droplets during the early stage of polymerization. Selvol 165 is used as a secondary suspending agent at 0.05–0.15 wt% on vinyl chloride monomer, in combination with a primary high-hydrolysis grade at 0.1–0.3 wt%. The aqueous phase is charged to a jacketed reactor equipped with a three-blade retreat-curve impeller and a baffle configuration that maintains a tip speed of 2.5–4.0 m/s; the vinyl chloride monomer is dispersed at 20–30 °C before the reactor is heated to 55–65 °C. Polymerization is initiated with a peroxydicarbonate or peroxyester initiator and proceeds under pressure of 0.8–1.2 MPa until conversion reaches 85–90%. At the stripping and drying stage, PVC slurry is passed through a continuous stripper at 80–100 °C and 20–40 kPa absolute pressure to reduce residual vinyl chloride. The dry resin is cooled to 40 °C before silo storage to prevent thermal degradation. Selvol 165 contributes to free-flowing powder with bulk density specifications measured by ISO 60:1977. The terminal product type is suspension PVC resin for rigid pipe, fittings, window profiles, and calendered sheet. Regulatory alignment includes EU REACH 1907/2006 with downstream PVC pipe assessed under EN 1401:2009 and residual VCM measured by ISO 6401:2022. This application does not fall under FDA food-contact permissions unless the downstream PVC article is separately evaluated under 21 CFR 177.1980 and the polymer complies with residual VCM limits specified in 21 CFR 177.1980(b).
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SELVOL Polyvinyl Alcohol 165 is a fully hydrolyzed, medium-viscosity polyvinyl alcohol resin supplied by Sekisui Specialty Chemicals. The material is identified by CAS 9002-89-5 and is normally supplied as a white to cream granular solid. Viscosity is specified as 5.2–6.2 mPa·s for a 4% aqueous solution at 20°C; degree of hydrolysis is controlled between 98.0–99.0 mol%. The residual acetate content therefore falls in the range of 1–2 mol%. Volatiles are limited to ≤5.0%, ash to ≤0.5%, and aqueous solution pH to 5.0–7.0. Viscosity and hydrolysis are assessed by the methods of JIS K6726, with ash determined by muffle-furnace ignition at 800°C and volatiles by oven drying to constant mass. The grade is not cold-water soluble; complete dissolution requires mechanical dispersion in water and heating to 85–90°C with low-shear agitation until no gel particles remain visible on a Hegman gauge. The product is selected for textile warp sizing, paper surface sizing, emulsion polymerization, remoistenable adhesives, and water-soluble film where a balance of film strength and handling viscosity is required.
In comparison with partially hydrolyzed polyvinyl alcohols of equivalent solution viscosity, SELVOL Polyvinyl Alcohol 165 produces adhesive films with lower equilibrium moisture uptake and higher tensile strength. The hydrolysis window of 98.0–99.0 mol% permits dense interchain hydrogen bonding after water evaporation; film tensile properties are assessed by ASTM D882-18 on cast films conditioned at 23 ± 2°C and 50 ± 5% relative humidity, and water absorption is measured by ASTM D570. Blocking resistance under storage loads is measured by ASTM D3354, with fully hydrolyzed grades typically showing lower blocking force than partially hydrolyzed grades at equivalent plasticizer content. The tradeoff occurs during application: substrate wetting on low-energy polymer films must be verified by wetting-tension solutions per ASTM D2578 because the 98.0–99.0 mol% hydrolyzed resin has higher aqueous surface tension than 87–89 mol% hydrolyzed resins. In addition, full dissolution requires water temperatures above 80°C, while partially hydrolyzed resins may hydrate at 40°C or below. These properties make the grade more suitable for films requiring water resistance and block resistance than for formulations requiring low-temperature cleanup.
During vinyl acetate/ethylene emulsion polymerization in a jacketed stainless-steel reactor equipped with a retreat-curve impeller, SELVOL Polyvinyl Alcohol 165 is typically charged as a predissolved 5–8% aqueous solution. Polymerization temperature is commonly maintained at 70–80°C while the PVOH acts as a protective colloid, controlling particle nucleation and preventing coalescence. The 5.2–6.2 mPa·s viscosity at 4% solids permits transfer with a diaphragm or progressing-cavity pump without excessive line pressure, while the hydrolysis range provides graft-site density for steric stabilization. Process control becomes critical after the initiator feed begins: excessive grafting onto the PVOH raises latex viscosity and forms macro-gel particles that are retained on a 150 μm screen; insufficient grafting leaves free PVOH in the serum and can allow particle aggregation during residual monomer stripping. The medium viscosity of the grade reduces agitator torque compared with high-viscosity fully hydrolyzed PVOH at equal charge, which is relevant in large reactors where agitator load defines the upper solids limit. Ash control at ≤0.5% narrows the influence of buffering salts on persulfate initiator decomposition; batch-to-batch shifts in ash can otherwise appear as variation in latex particle-size distribution. Published data specific to SELVOL Polyvinyl Alcohol 165 in ethylene-rich or crosslinking-comonomer formulations are limited; plant verification is required when the comonomer system departs from standard vinyl acetate/ethylene parameters or when multifunctional monomers are present.
When storage relative humidity exceeds 60%, SELVOL Polyvinyl Alcohol 165 takes up atmospheric moisture. The granular solid may then become inconsistent in loss-in-weight feeding, and the equilibrium moisture content can rise above the volatiles limit of 5.0%. Pre-drying at 60–80°C for 2–4 h in a circulating-air or desiccant dryer is recommended when the moisture content is found to be above 0.5% by gravimetric analysis. Drying above 100°C should be avoided because localized thermal history can yellow the resin. In cold-weather plants, makeup water below 20°C lengthens the swelling phase; a jacketed mixing vessel is preferred over direct steam sparging, which can generate foam and gel particles at the sparge point. The dissolution temperature is held at 85–90°C for 30–60 min, and the solution is then screened through a 150–250 μm basket strainer. Addition of the dry polymer to high-shear mixers at temperatures below 60°C is a known source of fish-eye agglomerates that resist later dispersion. Once dissolved, the solution must be used or preserved: microbiological degradation in unpreserved PVOH solutions occurs readily at 20–35°C, so holding times beyond 48 h require a compatible biocide. Borate ions, boric acid, and borax are incompatible with stable Newtonian handling because the 1,3-diol units form reversible but strong borate ester crosslinks, producing thixotropic gels or insoluble networks.
Aqueous paper surface-sizing formulations use SELVOL Polyvinyl Alcohol 165 to increase surface strength without the same degree of sheet closing observed with high-level starch-only formulas. The 4% solution viscosity permits metering-rod or puddle press application at solids of 2–6%, depending on sheet absorbency and size-press configuration. Oil and grease resistance of conditioned sheets is evaluated with TAPPI T 559; the fully hydrolyzed resin contributes barrier integrity when the sheet exits the after-dryer above 90°C. The grade can be blended with oxidized or modified starch to increase film flexibility and reduce formulation cost, but phase separation must be verified when the total solids exceed 15% because high-molecular-weight starch fractions may reduce homogeneity under shear. In textile warp sizing, the resin provides abrasion resistance after drying, low ash after singeing, and removal in hot water at 70–90°C during desizing. Size add-on is determined gravimetrically on the warp sheet, and the desired add-on range is set by loom speed, yarn hairiness, and humidity rather than by universal fixed values.
Viscosity differences among fully hydrolyzed polyvinyl alcohol grades alter solution handling, wet film thickness, and drying rate. SELVOL Polyvinyl Alcohol 165 occupies an intermediate position: it gives higher aqueous viscosity and film strength than lower-molecular-weight fully hydrolyzed grades, but it dissolves more rapidly and imposes lower mixer torque than high-viscosity grades. For absorbent substrates, a lower-viscosity grade penetrates more deeply but lowers film tensile strength as measured by ASTM D882-18. A higher-viscosity grade increases final film toughness but limits the maximum pumpable solids in diaphragm and progressing-cavity transfer lines. The specification envelope and process-relevant limits for SELVOL Polyvinyl Alcohol 165 are summarized in the table below.
| Parameter | Value | Method/Equipment |
|---|---|---|
| Degree of hydrolysis | 98.0–99.0 mol% | Residual acetate titration, JIS K6726 |
| Viscosity, 4% aqueous, 20°C | 5.2–6.2 mPa·s | Brookfield viscometer, JIS K6726 |
| Volatiles | ≤5.0% | Oven drying to constant mass |
| Ash | ≤0.5% | Muffle furnace ignition, 800°C |
| pH | 5.0–7.0 | Aqueous solution pH |
| Residual acetate | 1–2 mol% | Calculated from degree of hydrolysis |
In cast water-soluble film production, the 98.0–99.0 mol% hydrolysis level of SELVOL Polyvinyl Alcohol 165 yields high oxygen barrier at low relative humidity. Oxygen transmission rate is measured by ASTM D3985 on conditioned film; barrier performance degrades as relative humidity increases because water acts as a plasticizer in the amorphous phase. Film formulations intended for high-humidity service therefore require multilayer structures, barrier coatings, or crystallinity enhancement through orientation and heat setting. The medium viscosity of the grade allows casting from aqueous solution at practical solids while maintaining enough film tenacity after drying for orientation on a tentering line. Plasticizer is usually required at 5–15 phr to prevent brittleness; the exact level is determined by tensile testing per ASTM D882-18 and by tear strength per ASTM D1922. Cold-water solubility of the resulting film is limited below 40°C, so the grade is less suitable for rapid dissolution in cold water than lower-hydrolysis grades, but it is selected when the film must remain intact in humid handling environments and still dissolve in hot water.
For food-contact applications, compliance is determined by end-use conditions and must be confirmed against the manufacturer’s regulatory statement. Polyvinyl alcohol is recognized in FDA 21 CFR 175.105 for adhesives and 21 CFR 176.170 for components of paper and paperboard in contact with aqueous and fatty foods, subject to the limitations in those sections. The resin is not a direct food additive and must not be used as such. In electronic-grade or high-purity ceramic processes, residual ash and volatiles must be rechecked against the ≤0.5% ash and ≤5.0% volatiles lot data because thermal decomposition residues can affect downstream electrical or sintering performance.