| HS Code | 804216 |
| Product Name | SY-3000 Fatty Alcohol Defoamer for Papermaking |
| Appearance | Milky white liquid |
| Active Substance Content | 30% |
| Ph Value 1 Aqueous Solution | 6.5-8.0 |
| Viscosity 25 C | 800-1500 mPa·s |
| Density 25 C | 0.90-1.00 g/cm³ |
| Solubility | Dispersible in water |
| Ionic Type | Nonionic |
| Flash Point | >100°C |
| Foam Suppression Rate | ≥90% |
| Defoaming Time | ≤30 seconds |
| Recommended Temperature Range | 20-90°C |
| Storage Stability | Stable under normal storage conditions |
As an accredited SY-3000 Fatty Alcohol Defoamer for Papermaking factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | SY-3000 Fatty Alcohol Defoamer for Papermaking is supplied in 200 kg plastic drums, sealed for safe storage and easy handling. |
| Container Loading (20′ FCL) | 20′ FCL loaded with SY-3000 fatty alcohol defoamer, shrink-wrapped drums/pails, palletized securely, net weight optimized for container capacity. |
| Shipping | SY-3000 Fatty Alcohol Defoamer is shipped in sealed 200L drums or 1000L IBCs, protected from moisture and contamination. Classified as non-hazardous for road, sea, and air transport. Keep containers upright, dry, and away from extreme heat or freezing during transit and storage. |
| Storage | Store SY-3000 in a cool, dry, well-ventilated area away from direct sunlight, heat, and open flames. Keep the container tightly sealed to prevent contamination and evaporation. Recommended storage temperature is 5–35°C; avoid freezing. With proper handling, shelf life is approximately 12 months. |
| Shelf Life | Shelf life: 12 months when stored sealed in a cool, dry place away from direct sunlight. |
In brown stock washing, SY-3000 is injected into the filtrate return line rather than directly into the blow tank. The fatty alcohol defoamer is selected for this position because black liquor at 70–90 °C and pH 12–13 generates foam stabilized by tall oil soap and residual kraft lignin, not by free air alone. Rotary vacuum drum washers and single or double-roll presses lose displacement efficiency when foam accumulates in the filtrate pan; the air fraction in the mat reduces hydraulic conductivity and increases sodium carryover to the bleach plant. A representative addition level for northern softwood kraft is 0.1–0.5 kg/t oven-dry pulp, with the lower third of the range used on hardwood furnish containing less resin acid soap. Addition is split between the washer shower water header and the filtrate tank inlet to control foam both on the drum surface and in the pump suction. The finished product is unbleached kraft pulp at 10–16 % consistency exiting the final press, with residual black liquor solids washed to less than 15 kg Na₂SO₄/t pulp in modern fibre lines. Drainage performance is measured according to ISO 5267-1, and filtrate solids are analysed against the mill mass balance. Black liquor foam control must be balanced against evaporator carryover: free fatty alcohol can alter black liquor viscosity and deposit on surface condenser tubes if the defoamer is overdosed for more than 72 h continuously. For food-contact kraft, the complete formulation must be checked against 21 CFR 176.210 since emulsifiers and preservatives in the commercial product require mill-specific clearance.
Injection is made with a diaphragm metering pump fitted with a pulsation dampener; the product is diluted with process water at 1:5 to 1:20 before a static mixer. Slug feeding is avoided because foam height in the filtrate tank responds within 20–30 min, and uneven addition creates washer mat defects. For hardwood lines with low resin acid soap concentrations, the lower end of the dosage range is often sufficient, whereas softwood lines carrying soap separation tank overflow may require the upper end during spring and early summer when extractives levels are elevated. Foam height is measured by capacitance probes, and the defoamer pump is interlocked with the washer shower water flow to avoid addition during shutdown flushing.
Alkaline peroxide brightening of TMP and CTMP operates at 10–15 % consistency, 70–85 °C, initial pH 10.5–11.5, and retention times between 60 min and 120 min. Foam in the medium-consistency pump and tower is generated by peroxide decomposition oxygen, residual wood resin, and released anionic extractives. SY-3000 is added before the MC pump at 0.2–0.8 kg/t oven-dry pulp, usually split 70 % to the pump suction and 30 % to the tower discharge line. The defoamer collapses air pockets inside the pulp mat, allowing the alkaline peroxide liquor to contact the fibre uniformly and preventing brightening reversal caused by localised oxygen blanketing. The resulting furnish is bleached chemithermomechanical pulp with brightness targets of 70–80 % ISO depending on wood species; brightness is tested according to ISO 2470-1. Overdosing above 1.0 kg/t is not recommended because free fatty alcohol may precipitate with sodium silicate and form calcium soap deposits on the bleach tower outlet screw. Sodium silicate at 1.5–3.0 % on oven-dry pulp and DTPA at 0.1–0.2 % are compatible, but the mill must verify that residual defoamer does not reduce peroxide stabilisation; published peroxide residual data for SY-3000 in this exact configuration is limited.
The defoamer must remain stable in the alkaline peroxide liquor at high temperature. Phase separation in the dosing line is checked by turbidity meter; emulsion droplets larger than 10 µm can create localised darkening in the finished BCTMP bales due to carryover. The final pulp is dewatered through a twin-roll press and fluffer before baler; residual defoamer must not increase biological oxygen demand in the press filtrate beyond the mill discharge permit. COD increase is typically not measurable at 0.5 kg/t, but each mill must verify the effect against its own activated sludge kinetics and discharge permit limits.
On alkaline fine paper machines, the wet end operates at pH 7.5–8.5, headbox consistency 0.6–1.2 %, and wire pit temperature 40–50 °C. Foam accumulates in the wire pit, tray water, and seal pit because cationic starch, AKD/ASA size, and anionic trash form surface-active complexes. SY-3000 is introduced at 0.05–0.15 kg/t dry fibre for woodfree fine paper and at 0.1–0.3 kg/t for recycled linerboard; addition is split between the wire pit return and the fan pump suction. Defoamer addition changes the air content in the headbox from 0.8–1.5 % by volume to below 0.4 %, which is monitored by an M-porosity sensor or by vacuum drainage testing with a Dynamic Drainage Analyzer at 10 kPa vacuum. Sheet formation is evaluated by beta formation index and by TAPPI T 205 handsheets. Overdosing beyond 0.5 kg/t on closed white water systems creates a competing hydrophobic surface that can reduce cationic retention aid efficiency and cause size reversion when ASA is used; the size test according to TAPPI T 530 Hercules size is used to confirm no loss. The split ratio between wire pit and fan pump suction must be changed when broke furnish increases. Broke from coated paper releases more surface-active coating binder; the defoamer demand can double within 30 min after a grade change. On high-speed tissue machines with crescent formers, the defoamer is added to the machine chest rather than the wire pit because the short circulation loop has a residence time of 5–10 min and foam can reach the headbox before chemical response. The target is to maintain headbox air content below 0.3 % by volume.
| Paper grade | Addition point | Typical SY-3000 dose | Wet end temperature | Critical control limit |
|---|---|---|---|---|
| Alkaline woodfree fine paper | Wire pit return | 0.05–0.15 kg/t dry fibre | 40–50 °C | ASA sizing retention drop above 0.2 kg/t |
| Recycled linerboard / medium | Tray water return | 0.1–0.3 kg/t dry fibre | 45–55 °C | Anionic trash demand variability by furnish batch |
| Deinked tissue | Machine chest suction | 0.2–0.5 kg/t dry fibre | 30–45 °C | Wet strength resin retention loss above 0.6 kg/t |
| Coated base paper | Seal pit | 0.05–0.2 kg/t dry fibre | 35–45 °C | Pinhole formation if air content exceeds 0.6 % |
Post-flotation deinking lines using recovered office paper and old newsprint do not receive SY-3000 in the flotation cells. Residual defoamer in the flotation cell can reduce ink-laden foam overflow and decrease brightness gain by retaining hydrophobic ink particles in the accept stream. The application point is moved to the washer and thickener feed after the final flotation stage. Dosage on the washed recycled furnish is 0.05–0.2 kg/t dry fibre, adjusted to keep foam height in the wash filtrate tank below 30 cm; stock temperature is 40–50 °C and pH in the alkaline loop is 7.0–9.0. The defoamer controls fatty acid soap foam generated by saponified flexographic inks and coating binders. Residual ink is measured according to ISO 22754 or the ERIC method; effective residual ink concentration must remain below 250 mg/kg for deinked market pulp. Finished product includes recycled copy paper, tissue, and white-top linerboard. Overdosing above 0.3 kg/t can re-disperse ink into white water and increase dirt count; TAPPI T 213 dirt count is used for confirmation. A mill producing deinked market pulp from mixed office waste often sees defoamer demand peak after alkaline soak and dispersion, not after flotation. The dosage is then split between the disperser discharge and the post-bleaching washer. The use of SY-3000 after flotation must be validated by ERIC and brightness measurements because over-deaeration of wash filtrate can reduce the removal of microstickies; if ERIC increases by more than 50 mg/kg against the control, the dosage is reduced.
At the size press, oxidised or enzyme-converted starch is held at 55–70 °C and pH 6.0–8.5. Foam in the starch circulation tank causes film splitting defects, rod lines, and starch pickup variation. SY-3000 is added to the cooked starch storage tank at 0.01–0.05 % on dry starch solids, or 0.05–0.20 L/t of surface size, before the supply pump. The defoamer reduces foam height without reducing surface tension to the point where the starch film dewets; pickup is measured on the size press by gravimetric difference and should remain within ±0.3 % absolute of the target. The finished sheets are converted into corrugated board, gypsum liner, or office paper. A compatibility issue arises when the defoamer is mixed with cationic starch at high pH after alum addition; cationic starch may precipitate with free fatty alcohol, creating white deposit on the drying cylinders. Foam collapse time is screened by ASTM E2407-04. Published mill-scale correlation for SY-3000 in enzyme-converted starch systems is limited; laboratory Ross-Miles foam height data should be confirmed in the circulating loop. Rod lines and starch foam are often confused with coater streak defects; the distinction is made by measuring foam rise in a graduated cylinder with recirculated starch at 60 °C. If static surface foam collapses within 15 s after SY-3000 addition but film splitting persists, the defect is rheological rather than foam-related. This diagnostic prevents unnecessary defoamer overdosing and reduces the risk of deposit on the first dryer cans. Converted sheet properties measured by ISO 2758 burst strength should not change outside mill variability.
Closed white water circuits with save-alls or dissolved air flotation units process suspended solids loads from 500 mg/L to 5,000 mg/L at hydraulic loading rates of 5–15 m/h. Surface foam generated by residual sizing agents, starch, and anionic trash reduces clarifier efficiency and causes TSS carryover into clarified white water. SY-3000 is dosed into the DAF inlet line at 1–3 mg/L on total flow, upstream of the flocculation tube but downstream of dissolved air injection. The fatty alcohol defoamer collapses surface foam without producing mineral-oil sheen; clarified water TSS is verified by gravimetric analysis according to ISO 11923. Sludge solids from the DAF float are pressed to 25–40 % consistency and either returned to furnish or sent to disposal. Overdosing above 5 mg/L interferes with cationic polyacrylamide flocculation and can increase effluent COD due to unbound fatty alcohol; jar testing with the specific polymer lot is required before changing the ratio. The terminal stream is clarified white water reused for machine showers, with fibre recovery rates of 90–95 % on a mass balance basis.
The dosing point relative to dissolved air injection is critical. If SY-3000 is injected before the pressure release valve, the defoamer may depressurize partially and form an emulsion layer in the white water tank. If injected after the flocculation chamber, the surface foam collapses but the fine fibre flocs are not protected from air bubbles in the flotation zone. A split dose of 70 % upstream of the flocculator and 30 % onto the DAF surface is used when surface foam persists. The DAF float solids and clarified water quality are monitored by on-line turbidity and weekly gravimetric TSS; a turbidity value below 50 NTU is commonly required for shower water reuse.
| Standard | Application relevance | Measurement or limit |
|---|---|---|
| ISO 5267-1 | Drainage after defoamer addition | Schopper-Riegler number change |
| ISO 2470-1 | Mechanical pulp brightness | 70–80 % ISO |
| ISO 22754 | Residual ink after deinking | ERIC below 250 mg/kg |
| TAPPI T 530 | Size reversion control | Hercules size retention time |
| TAPPI T 213 | Dirt count in recycled furnish | Visual dirt count in finished sheet |
| ASTM E2407-04 | Defoamer efficacy screening | Foam collapse time in seconds |
| 21 CFR 176.210 | Food-contact paper defoamer clearance | Formulation-specific verification |
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SY-3000 Fatty Alcohol Defoamer for Papermaking is a water-dispersible, non-silicone formulation intended for the reduction of entrained air and surface foam in paper machine wet-end systems operating under alkaline conditions. The active phase is based on long-chain fatty alcohols, typically C16–C22 saturated and unsaturated fractions, compounded with nonionic emulsifiers and stabilizers. This composition class is selected where the process requires bubble collapse without adding mineral oil extractives or persistent silicone residues to white water. The supplier’s current technical data sheet and certificate of analysis should be consulted for batch-specific values. For fatty alcohol defoamers of this category, the following control intervals are typically used for incoming inspection and comparison of supplied batches.
| Property | Test method or basis | Typical range | Operational note |
|---|---|---|---|
| Density at 25°C | ISO 2811-1:2023 | 0.85 g/cm³ to 1.05 g/cm³ | Confirms emulsion phase stability and storage handling |
| pH as supplied | ISO 976:2021 | 5.0 to 8.0 | Measured on neat emulsion with glass electrode |
| Active content | Supplier method based on non-volatile residue | 10–30 wt% | Higher active content does not automatically indicate higher efficiency |
| Dynamic viscosity | ISO 2555:2023 | 200–2000 mPa·s at 25°C | Brookfield LV spindle at 60 rpm; shear history affects reading |
| Shelf life | Manufacturer storage stability data | 6–12 months | Avoid freeze-thaw cycles and direct steam tracing |
These values are class-typical control intervals and should not be regarded as SY-3000 specifications unless confirmed by the manufacturer for a specific batch. Published data specific to SY-3000 is limited; therefore, any acceptance limit proposed for a paper machine must be derived from the supplier’s current certificate of analysis and from mill-side pre-shipment samples.
The operational boundary for SY-3000 is governed by the interaction between the dispersed fatty alcohol phase and the wet-end charge environment. In woodfree fine paper furnishes containing precipitated calcium carbonate at pH 6.5–8.5 and a headbox temperature of 35–55°C, the defoamer must survive shear in the fan pump and pressure screen while retaining enough droplet size to spread at the air–water interface. When the wet-end is highly anionic due to dissolved and colloidal substances, the nonionic emulsifier system generally resists electrostatic precipitation, but the active phase can still partition onto fibre fines and filler surfaces. That partition reduces the quantity of defoamer available for bubble destabilization and is one reason the addition point must be positioned close to the headbox approach system rather than in the machine chest.
Cationic retention aids and cationic starch can interact with the stabilizer system if the two streams are mixed without adequate separation. SY-3000 should be injected into the thin stock loop at a point where high-charge cationic polymers have already been diluted, or with a residence-time buffer before contact. Contact between concentrated fatty alcohol emulsion and strong cationic fixative solutions can demulsify the product and form tacky deposits on approach piping. Avoid simultaneous addition of oxidizing biocides at the same injection quill. The product should not be stored below 0°C or above 40°C for prolonged periods. Thermal damage above 50°C is a known failure mode for wax-based fatty alcohol emulsions because it can induce coalescence and loss of redispersibility. For mills using hot process water, dilution water temperature should be within 5°C of the thin stock temperature to avoid thermal shock.
The defoamer is not a deposit-control agent. If hydrophobic pitch, stickies, or white pitch are present at high concentration, the fatty alcohol phase may migrate into those hydrophobic particles. This can reduce defoaming efficiency and increase the size of aggregated hydrophobic material. The interaction should be examined by measuring headbox air content with TAPPI T 281 and by monitoring white water turbidity using ISO 7027-1:2016 before and after dose changes.
When a gap former operates above 1000 m/min with filler loading above 20% by mass, entrained air bubble size distribution in the approach system becomes a measurable process variable. On such machines, SY-3000 is typically diluted in process water at a ratio between 1:10 and 1:20 before continuous dosing into the fan pump suction or the headbox mixing line. A diaphragm or peristaltic metering pump with low dead volume and backpressure control is used. Dosing lines should slope continuously to the injection point to prevent separation in stagnant low-flow zones. The addition point downstream of the pressure screen, in the headbox recirculation line, or at the white water return fed to the fan pump inlet provides more direct air removal in gap former loops than addition at the pulper or machine chest.
Dose response for fatty alcohol defoamers is usually steep. Starting trials on fine paper machines are commonly conducted at 0.02–0.10 kg active product per tonne dry fibre, adjusted in 10–20% increments while headbox air content is measured by TAPPI T 281. This range is an operating reference and is not a confirmed SY-3000 specification. On high-speed machines, dose changes should be separated by at least 30 min to allow the white water loop to reach a new steady state. Overfeed conditions may appear as increased pinholes, surface defects, and unstable drainage because excess dispersed hydrocarbon phase can depress sheet quality. Underfeed conditions appear as persistently elevated headbox air content and visible foam accumulation in wire pit and tray water.
In recovered fibre systems, white pitch and hot-melt adhesive carryover can alter the performance of any hydrophobic defoamer. SY-3000 may co-adsorb onto these hydrophobic surfaces because the fatty alcohol active phase has higher affinity for low-energy hydrophobic solids than for the aqueous phase. This co-adsorption can reduce the effective defoamer concentration and create larger sticky aggregates that appear as deposits on forming fabrics and press felts. The risk is higher in mixed waste paper and old corrugated container stock than in bleached woodfree furnishes. For recycled paper machines, the product is best evaluated in a side-stream loop containing pressure screen rejects, white water from a disc filter, and controlled aeration. If stickies control agents are already present, the combined effect should be assessed because some formulations may produce larger hydrophobic aggregates.
The interaction is usually monitored by measuring headbox air content via TAPPI T 281, white water turbidity via ISO 7027-1:2016, and macro-stickies deposition on a forming fabric coupon. A rise in turbidity after defoamer addition does not automatically indicate defoamer failure; it may indicate partition into pre-existing hydrophobic material. If the particle size distribution of white water solids shifts upward, the defoamer feed point may need to be moved downstream or the dose reduced below the threshold that generates continuous free oil films. No single laboratory foam collapse test can replace this approach because the interaction is machine-loop dependent.
The differentiation between SY-3000 and other defoamer classes is not governed by a single test but by combined measurements of headbox air content, white water turbidity, sheet defect maps, and retention stability. Silicone emulsions usually provide faster spread and lower active dosage, but the resulting polydimethylsiloxane droplets can remain in the wet end and contribute to pinholes, print mottle, and deposition on forming fabrics if the machine cannot tolerate persistent silicone. Mineral oil defoamers provide broad suppression of surface foam but increase solvent-extractable material in process water and may increase biological oxygen demand. Fatty alcohol defoamers such as SY-3000 occupy an intermediate position: defoaming speed is generally slower than a strong silicone emulsion, while the lower persistence in white water and lower deposit tendency are often preferred on alkaline fine paper machines using retention aids and synthetic sizing agents.
| Attribute | SY-3000 fatty alcohol class | Silicone emulsion | Mineral oil defoamer |
|---|---|---|---|
| Active phase chemistry | Long-chain fatty alcohol/wax | Polydimethylsiloxane | Mineral oil and hydrophobic solids |
| Knockdown speed in paper stock | Intermediate; requires fine dispersion | Fast; low active dose often sufficient | Intermediate to fast depending on solid content |
| Persistence in white water | Moderate; may require continuous dosing | High; can accumulate in loops | Medium to high; extractive loading increases |
| Deposit tendency on forming fabric | Lower when dosage is controlled | High if overfed or shear-damaged | Moderate to high; can bind pitch and fines |
| Biodegradability of active phase | Fatty alcohol actives show ready biodegradability in OECD 301F read-across | Not readily biodegradable | Not readily biodegradable |
| Typical application pH | 6.5–8.5 common for alkaline wet end | Broad, but emulsion stability varies with cationic demand | Broad, but extractive impact limits use in fine paper |
The comparison above is based on public industrial data and class chemistry. It does not replace a direct mill trial because the relative ranking can shift with furnish type, dosage, shear history, retention program, and machine speed.
Because the foaming tendency of recovered fibre lines is driven by starch, soap, and hydrophobic contaminants, the SY-3000 dose established on a woodfree fine paper machine cannot transfer directly to a liner or corrugating medium machine. On old corrugated container and mixed waste paper stocks, pulper carryover and dissolved air flotation unit inefficiencies can increase defoamer demand. SY-3000 should be evaluated in a side-stream loop that includes pressure screen rejects, white water from a disc filter, and aeration under controlled shear. Where stickies control agents are already present, the combined effect should be assessed because some formulations may produce larger hydrophobic aggregates. Avoid simultaneous injection of SY-3000 with high-charge cationic fixatives, concentrated oxidizing biocides, or hot process water above 50°C, because these conditions can destabilize the emulsion before the active phase reaches the headbox. For food-contact paper grades, the supplier should confirm regulatory status under 21 CFR 176.170 and 21 CFR 176.180, as well as REACH registration for the final formulation.