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Glue Control Enzymes

    • Product Name: Glue Control Enzymes
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 667935
    Product Name Glue Control Enzymes
    Product Type Enzymatic adhesive remover
    Form Liquid concentrate
    Active Enzymes Protease and amylase blend
    Mechanism Breaks down adhesive polymers into water-soluble compounds
    Primary Use Removes glue, stickers, and adhesive residues
    Compatible Surfaces Glass, plastic, metal, wood, and fabric
    Application Method Spray or wipe directly onto affected area
    Dwell Time 5 to 15 minutes for effective action
    Dilution Ready-to-use or dilutable 1:10 with water
    Ph Range 7.0 to 8.5
    Biodegradability Readily biodegradable
    Storage Store in a cool, dry place away from direct sunlight
    Shelf Life 12 months from manufacture date
    Safety Non-toxic and non-irritating when used as directed

    As an accredited Glue Control Enzymes factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g container of Glue Control Enzymes, powder form, with tamper-evident seal, hazard label, and clear usage instructions.
    Container Loading (20′ FCL) 20′ FCL: Glue Control Enzymes packed in sealed drums, palletized and secured, one full container load ready for shipment.
    Shipping Glue Control Enzymes ship in insulated containers with cold packs to maintain stability. Packaging includes sealed, leak-proof containers to prevent contamination. No hazardous goods classification applies, but avoid extreme temperatures and direct sunlight. Expedited shipping recommended to ensure enzyme activity remains intact upon arrival.
    Storage Store Glue Control Enzymes in a tightly sealed original container in a cool, dry, well-ventilated area. Avoid direct sunlight, excessive heat, and moisture. For optimal enzyme stability, refrigeration at 2–8°C is recommended. Keep away from acids, oxidizers, and foodstuffs. Ensure container remains upright and clearly labeled.
    Shelf Life Store in a cool, dry place; shelf life is typically 12 months when unopened. Avoid moisture and heat.
    Application of Glue Control Enzymes

    What Limits Stickies Removal During Old Corrugated Container Repulping?

    In recycled containerboard mills operating on EN 643:2013 grade 1.04 and 1.05 old corrugated containers, the principal source of deposition and sheet defects is fragmented hydrophobic adhesive mass released during drum pulping. The enzyme preparation, standardised for esterase activity against tributyrin substrate at pH 7.0 and 40°C, is added continuously to pulper dilution water at 0.10–0.35 kg per tonne of oven-dry recovered fibre. The effective upper boundary for this enzyme class is 0.6 kg/t oven-dry fibre, beyond which anionic trash load rises and cationic retention aid demand increases without a corresponding stickies reduction. The enzyme cleaves acetyl ester bonds in polyvinyl acetate and acrylic-ester copolymers, converting tacky hydrophobic domains into water-dispersible polyvinyl alcohol moieties and acetate. It does not hydrolyse the carbon-carbon backbone of styrene-butadiene rubber, ethylene-vinyl acetate, polyolefin, or crosslinked polyacrylate hot melts. Process placement is constrained by temperature and pH stability: dosing into the pulper must occur where stock temperature remains within 35–55°C and pH 6.5–8.0 for a retention time of 20–45 min. Injection after high-density cleaning into an alkaline chest above pH 9.0 reduces enzyme half-life to less than 15 min under typical mill conditions. The downstream sequence—0.15 mm slotted fine screens, forward centrifugal cleaners, thickening, and disc dispersion at 80–100°C—removes non-degraded film fragments but cannot return micro-stickies already deposited on fibre surfaces. Macro-stickies concentration in the accepts is monitored by TAPPI T 277; image analysis for visible stickies and plastics follows ISO 15360-2:2015. Finished products include recycled testliner and corrugating medium for containerboard. Food-contact containerboard compliance is verified through extractive limits in FDA 21 CFR 176.170(c) and EU 1935/2004; the enzyme itself is handled under the REACH eSDS. Simultaneous addition of sodium hypochlorite or peracetic acid in the same injection point is incompatible because oxidative residuals inactivate the esterase before it can act on adhesive surfaces.

    Standard or RegulationScope Relevant to Recovered ContainerboardApplication in Enzyme Treatment
    EN 643:2013Recovered paper and board gradesInput fibre classification for OCC and mixed recovered grades
    TAPPI T 277Macro-stickies in process waterProcess water monitoring before and after enzyme dose
    ISO 15360-2:2015Image analysis for stickies and plastics in recycled pulpFinished stock quality control after fine screening and dispersion
    FDA 21 CFR 176.170(c)Food-contact paperboard extractive limitsFinished containerboard compliance
    REACH (EC) No 1907/2006Substance registration, eSDS, exposure limitsHandling, dosing system design, worker safety

    In tissue mills operating on 100% recovered paper, adhesive-based defects appear as fibre protuberances and holes at the Yankee creping blade rather than as visible sheet dirt. The esterase-containing preparation is dosed into the high-consistency pulper or coarse screening feed chest at 0.15–0.30 kg per tonne of oven-dry furnish when the incoming bale mix contains pressure-sensitive label stock and recycled office waste. The dose is adjusted downward for bales dominated by silicone release liners, ethylene-vinyl acetate backings, or oxidised hot melt fragments because these substrates are not enzyme-degradable. The downstream tissue process—pulping at 4–5% consistency, deinking flotation for white grades, disk refinement, crescent former wet end, and Yankee dryer with creping doctor—generates hood temperatures above 350°C, but the enzyme has already been denatured in the dryer section and its reaction is confined to liquid-phase stock. Compliance for low-basis-weight tissue, kitchen towel, and napkin grades that may contact dry foods follows FDA 21 CFR 176.170 and EU 1935/2004; finished article total nonvolatile extractive testing is conducted under FDA 21 CFR 176.170(c). The enzyme itself is handled under the REACH eSDS. When pulping is carried out above pH 8.5 or at temperatures above 65°C, enzyme half-life falls below 20 min, and a split-dose strategy into the pulper and post-screen chest is required to maintain deposit control on the Yankee surface.

    Corrugator Starch Adhesive Viscosity Drift, Gel-Point Kinetics, and Enzyme Inactivation

    Corrugated board production consumes a two-component Stein-Hall starch adhesive in which the carrier starch is gelatinised with caustic soda and the raw starch slurry is mixed at the corrugator. The thermostable α-amylase component of the glue control enzyme range is used to reduce carrier starch molecular weight, but residual activity after gel point is the principal processing hazard. The addition ratio is set at 0.15–0.35 kg of enzyme per tonne of dry starch in the carrier phase, or 0.02–0.05% on dry starch, and is trimmed against a target Stein-Hall viscosity of 30–50 s at 61°C. The enzyme cleaves α-1,4-glycosidic linkages, lowers gelatinised carrier viscosity, and permits increased total starch solids without exceeding glue roll pick-up limits. However, the same activity must be fully denatured before the adhesive film reaches the single-facer glue roll; otherwise viscosity continues to fall after application, producing shallow bond lines, dry bond strength loss, and washboarding on the corrugator. Inactivation requires the carrier temperature to exceed 85°C for at least 10 min during cooking, or the addition of a food-grade acidulant to reduce pH below 5.0 after the carrier is fully hydrated. Equipment includes a jacketed carrier tank with turbine agitation, Stein-Hall cup, Brookfield RVT viscometer at 60 rpm, and automatic temperature logging. Finished product types are single-wall, double-wall, and triple-wall corrugated boards for food and industrial packaging. Food-contact corrugated board is subject to FDA 21 CFR 175.105 for the adhesive and FDA 21 CFR 176.170 for the paperboard, while EU member states require compliance with EU 1935/2004. Dry pin adhesion is assessed by TAPPI T 821; viscosity drift is tracked by Stein-Hall cup repeatability of ±2 s. Sodium hypochlorite residuals above 10 ppm in dilution water inactivate the enzyme before starch conversion and produce inconsistent carrier viscosity.

    Mixed office waste deinking lines that run alkaline pulping at pH 9.5–11.0 create a process window in which esterase performance is sharply reduced unless the formulation is alkali-tolerant. The glue control enzyme is applied at 0.20–0.40 kg per tonne of oven-dry recovered fibre into the buffered chest after coarse screening where pH is adjusted to 8.0–8.8 and temperature is held below 55°C. This placement avoids the strongest alkaline pulper environment and extends enzyme half-life. The mechanism reduces tack of polyvinyl acetate label residues and supports subsequent flotation removal by collector chemicals, but it does not substitute for alkaline soap flotation or post-flotation screening. Process equipment includes medium-consistency drum pulpers, coarse screens, multiple dissolved air flotation cells, forward cleaning, disc dispersion at 25–30% consistency, and reductive bleach towers. The production output is recycled copy paper, magazine stock, and preprint fillers. Compliance is verified through ISO 15360-2:2015 for residual visible stickies and EN 643:2013 for incoming recovered paper grades; where recycled content enters packaging grades, FDA 21 CFR 176.170 applies. A process conflict occurs when enzyme is dosed directly into the alkaline pulper: half-life falls below 15 min, and the resulting acetic acid release can transiently depress pH but not enough to compensate for activity loss. Published data for this specific configuration on mixtures of toner, hot melt, and polyvinyl acetate label residues remains limited; mill trials are required because toner and ethylene-vinyl acetate fragments are not enzyme substrates.

    When Molded Fiber Food Trays Demand Zero Visible Adhesive Specks

    Molded fibre plants converting recovered newsprint and kraft trimmings into egg cartons, cup carriers, and fruit trays face a specific specification: visual inspection rejects adhesive specks larger than 0.5 mm because brand owners require a clean food-contact surface. The esterase preparation is dosed at 0.10–0.25 kg per tonne of oven-dry fibre in the pulper or stock chest at 40–55°C and pH 6.5–7.8; the dose is selected using TAPPI T 277 macro-stickies counts after fine screening and TAPPI T 213 dirt count for visible specks in the formed sheet. The downstream process includes high-turbulence pulping at 3–4% consistency, pressure screening with 0.15–0.20 mm slots, vacuum forming into shaped wire moulds, and hot press drying at 160–220°C for 40–60 s. Enzyme action reduces tack of polyvinyl acetate-based label residues so they pass screens before they can smear across the mould wire; it does not remove charred or oxidised hot melt specks that have already been thermally fixed during upstream recycling. Compliance is dominated by FDA 21 CFR 176.170(c) for aqueous and fatty foods, EU 1935/2004, and BfR Recommendation XXXVI for paper and board food-contact materials. Terminal product types are egg cartons, cup carriers, food trays, and vineyard trays. An incompatibility exists with cationic starch and high-charge polyamine retention aids: dosing the enzyme into the machine chest while polyamine is present above 0.5 kg/t can form flocs that reduce sheet appearance, so enzyme addition should be completed before final retention aid application.

    Continuous deposition on forming fabrics and press felts in recycled board machines can be reduced by applying diluted enzyme directly to the return run of the forming fabric through low-pressure fan nozzles at 0.02–0.05 kg/t of total production, diluted at 1:500–1:1000 in mill water. The spray is applied before the suction boxes to allow contact with adhesive deposits while the wire returns to the headbox loop. This approach does not replace stock preparation enzyme dosing but reduces the interval between shutdowns for high-pressure shower cleaning of wet-end clothing. Typical process parameters are shower water temperature 35–50°C, pH 6.5–7.5, nozzle spacing 150–300 mm, and spray pressure 2–4 bar. The application is limited to machine clothing that is chemically compatible with enzyme solutions; polyurethane-based forming fabrics show no measurable hydrolysis under these short contact times, but repeated exposure above 60°C is avoided. Compliance for worker safety is managed under REACH (EC) No 1907/2006 and EU CLP Regulation (EC) No 1272/2008; the preparation is classified as a mist inhalant sensitiser, so enclosed dosing skids and local exhaust ventilation are required. Terminal products include all recycled board and paper grades produced on the machine, including containerboard, coreboard, and plasterboard liner. Published data for this specific configuration is limited because deposit reduction depends on fabric age, surface porosity, line speed, and the ratio of fresh to oxidised adhesive; therefore the dosage is established by monitoring fabric permeability and press section draw tension.

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    Certification & Compliance
    More Introduction

    Glue Control Enzymes is a technical liquid enzyme preparation supplied as GCE-1100 for hydrolytic control of ester-containing adhesive residues in recycled papermaking furnishes. The active enzyme is a thermostable esterase expressed in a non-toxigenic Aspergillus oryzae production host and formulated with a nonionic stabilizer. The released activity is 12,000 U/g measured by pH-stat titration with tributyrin substrate at 40°C and pH 7.0. The product is miscible with clarified mill water at 5–45°C and is intended for continuous injection into stock preparation lines processing 100% OCC, mixed office waste, or recovered tissue fiber.

    What Distinguishes GCE-1100 from Conventional Stickies Control Agents?

    Conventional treatments such as talc, bentonite, and cationic detackifiers act primarily by surface passivation or charge neutralization. Talc dosing in OCC systems typically ranges from 2 to 5 kg/t and leaves the adhesive mass intact while reducing tack on machine surfaces. Cationic detackifiers may aggregate fine stickies into larger complexes that are retained but not degraded. GCE-1100 follows a hydrolytic route: the esterase attacks ester linkages in polyvinyl acetate homopolymers, vinyl acetate-ethylene copolymers, acrylate ester copolymers, and certain polyester-based hot melts, cleaving the polymer backbone or pendant ester groups to generate lower-molecular-weight fragments with reduced film-forming capacity. The catalytic dose is typically 150–250 g/t of dry fiber, which is approximately 10 to 20 times lower than talc by mass. Charge demand shift at this dose is generally below 50 µeq/L as measured by polyelectrolyte titration with polyDADMAC and a Mütek PCD-04 detector.

    Catalytic scope is limited to ester-bearing adhesive components. Polyolefinic hot melts, silicone release coatings, and polyether-based polyurethanes do not contain hydrolysable ester bonds in the main chain and are unaffected by the preparation. For mixed furnishes with a high proportion of these materials, GCE-1100 must be combined with physical detackification or improved screening. The preparation is not a dispersant and does not permanently re-emulsify degraded stickies into the white-water loop; the lower-molecular-weight fragments partition into water and are removed with the sheet or effluent in accordance with the mill mass balance. Mill-specific furnish characterization by solvent extraction and Fourier-transform infrared spectroscopy is therefore recommended before dose finalization.

    Model GCE-1100 Release Specifications, Physical Handling Limits, and Storage Behavior

    ParameterRelease valueTest method
    AppearancePale amber to light brown liquidVisual
    Esterase activity10,000–14,000 U/gpH-stat tributyrin assay at 40°C, pH 7.0
    Protease side activity≤1,500 U/gAzocasein digestion, 40°C, 30 min
    pH as supplied6.3–7.2pH electrode
    Density at 20°C1.04–1.08 g/cm³ASTM D4052-22
    Viscosity at 25°C20–80 mPa·sBrookfield RVT spindle 2, 100 rpm
    Freeze-thaw recovery≥85% activity after 3 cyclesInternal freeze-thaw assay
    Storage stability≥90% activity after 12 months at 4–10°CAccelerated stability assay

    A higher-temperature variant, GCE-2100, is formulated for recycled newsprint and tissue lines operating between 60°C and 75°C; the declared esterase activity is 8,500 U/g at pH 7.0 and 65°C. Published data for GCE-2100 in high-temperature OCC lines is limited, and the standard GCE-1100 remains the default recommendation for pulper temperatures below 60°C.

    When Stock Temperature, pH, and Oxidative Biocide Residuals Exceed the Operating Envelope

    The catalytic window of GCE-1100 is pH 6.0–9.5, with optimum hydrolysis between pH 7.5 and 8.0. Stock temperature should be maintained between 35°C and 60°C; above 65°C irreversible denaturation proceeds rapidly, with residual activity falling below 25% within 30 min in buffered mill-water trials. Below 30°C, the reaction rate declines but the enzyme remains stable. Free chlorine residual above 0.5 mg/L or hydrogen peroxide residual above 25 mg/L at the injection point is incompatible; activity loss exceeds 50% within 10 min at pH 7.0 under these oxidant loads. Ozone-treated white water should not be used for dilution. Alum levels above 1,500 mg/L can flocculate the formulation carrier at pH below 5.8. In mills operating below this pH, the product should be injected into a neutralized or buffered chest upstream of alum addition.

    GCE-1100 Reduces Micro-Stickies in OCC Recycled Liner and Tissue Furnishes

    In recycled packaging and tissue mills, the preparation is used to reduce machine deposition from pressure-sensitive adhesives and hot melts entering with recovered fiber. The primary application point is the pulper or a stock chest after coarse screening. A contact time of 45–90 min at 40–60°C is required for measurable ester hydrolysis. The dose is typically 150–300 g/t of dry fiber, determined by laboratory loop trials and adjusted on the basis of machine deposit weight. Production-scale observations on gap-former recycled liner lines running 100% OCC at 900–1,300 m/min indicate that forming-fabric deposit weight can decrease by 40–65% after 7–14 days of continuous dosing when compared with an untreated control using gravimetric fabric coupon measurements. Sheet tensile index loss under ISO 1924-2 is generally below 3% at 250 g/t. Published data for this specific configuration is limited, and the observed degree of deposit reduction depends strongly on furnish age, adhesive type, and machine speed.

    Dilution and metering equipment should be selected for low-shear handling. A progressive-cavity pump with 4–20 mA speed control and a dilution-water rotameter is preferred, with the enzyme diluted 1:5 to 1:10 in clarified water at 20–40°C immediately before injection. The diluted solution should be used within 24 h to prevent microbial growth. Injection through a quill into the chest mixing zone or pump suction is acceptable; avoid adding into high-shear refiners or steam-heated lines above 65°C because thermal denaturation is not recoverable. Dosing interlocks tied to pulper conveyor weight and chest level improve consistency of grams-per-tonne delivery and prevent overdosing during furnish weight swings.

    Benchmark GCE-1100 Against Talc and Cationic Detackifiers Under Laboratory Screening Conditions

    Table 2 presents a controlled laboratory screening of 100% OCC repulped at 50°C and pH 7.2 with 45 min contact time. Macro-stickies were quantified according to ISO 15360-2 with a 0.15 mm slot screen; forming-fabric deposit weight was determined gravimetrically on stainless-steel coupons placed in a laboratory white-water loop for 24 h. Values are comparative for the same furnish and should not be transferred directly to mill conditions without validation.

    TreatmentDose (g/t dry fiber)Macro-stickies area (mm²/kg)Forming-fabric deposit weight (g/m²/24 h)Charge demand shift (µeq/L)
    Untreated control06,20018.60
    Talc dispersion2,0004,80016.1+15
    Cationic detackifier4003,9008.9−142
    GCE-11002507502.1−34
    GCE-1100 plus talc150 + 7504101.2−28

    The comparative screening data indicate that the enzymatic route reduces total macro-stickies area more than talc or cationic detackifier alone. Combined application of GCE-1100 with a reduced talc dose produces the lowest deposit weight in this furnish, but the economic optimum is mill-specific because freight, furnish composition, and effluent load differ. The product should not be used as a sole control measure when macro-stickies inlet load exceeds 10,000 mm²/kg; in such furnishes screening, mechanical removal, and furnish substitution should be evaluated in parallel.

    Compatibility with wet-end additives is generally acceptable within the stated pH and oxidant limits. At 250 g/t, Canadian Standard Freeness measured by ISO 5267-2 changes by less than 4%, and first-pass retention measured by dynamic drainage jar remains within ±1.5% of the baseline. The preparation is compatible with neutral and alkaline sizing agents, polyacrylamide retention aids, and bentonite microparticle programs. High anionic trash in the stock may temporarily complex with the enzyme stabilizer system and reduce available activity; furnish conductivity and cationic demand should be monitored when GCE-1100 is first introduced.

    The safety data sheet identifies the enzyme protein as a possible respiratory sensitizer if aerosolized. Local exhaust ventilation should be used during open transfer of totes or drums. The formulation is not classified for acute oral or dermal toxicity under REACH Annex II criteria, but direct skin contact with concentrated product should be avoided due to potential proteolytic side activity. Empty containers should be triple-rinsed and not reused for food contact. Direct food-contact suitability of the treated paper or board must be confirmed under FDA 21 CFR 176.170, EU Framework Regulation (EC) No 1935/2004, or applicable national codes. The preparation is not compatible with strong mineral acids, sodium hypochlorite, or prolonged storage above 40°C. Dispose of diluted or expired product in accordance with local biological waste regulations.

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