Sodium Hydroxide Caustic Soda Flakes 98% China

    • Product Name: Sodium Hydroxide Caustic Soda Flakes 98% China
    • 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 886324
    Product Sodium Hydroxide Caustic Soda Flakes 98% China
    Chemical Formula NaOH
    Cas Number 1310-73-2
    Purity 98%
    Appearance White flakes
    Odor Odorless
    Molecular Weight 40.00 g/mol
    Solubility In Water 109 g/100 mL at 20°C
    Ph 1 Solution 13-14
    Melting Point 318°C (604°F)
    Boiling Point 1388°C (2530°F)
    Density 2.13 g/cm³ at 25°C
    Grade Industrial/Caustic Soda Flakes
    Country Of Origin China

    As an accredited Sodium Hydroxide Caustic Soda Flakes 98% China factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25kg net in double-layer PP woven bags with PE liner, palletized and shrink-wrapped for safe transport.
    Container Loading (20′ FCL) 20′ FCL loaded with ~25 MT Sodium Hydroxide Flakes 98%, packed in 25kg bags, palletized, secured, kept dry and ventilated.
    Shipping Shipping Sodium Hydroxide Caustic Soda Flakes 98% (China) requires strict compliance. Classified as a corrosive (UN 1823, Class 8), it ships in sealed, moisture-proof bags within ventilated or standard containers. Avoid aluminum containers; use steel or plastic-lined. Ensure segregation from acids and foodstuffs. Proper labeling, IMDG documentation, and temperature/dryness controls are essential for safe international transport.
    Storage Store sodium hydroxide flakes in a cool, dry, well-ventilated area inside tightly sealed, moisture-proof containers. Keep away from acids, organic materials, metals like aluminum, and water sources. Protect from humidity and physical damage. Use proper PPE when handling. Under correct conditions, shelf life is typically 12–24 months.
    Shelf Life Shelf life is approximately 2 years when stored sealed, dry, and away from moisture and carbon dioxide.
    Application of Sodium Hydroxide Caustic Soda Flakes 98% China

    In alumina refining, caustic soda flakes from China with an NaOH assay of 98.0% are dissolved into recirculated spent liquor rather than into raw water. Make-up rate is set by the molar Al2O3/Na2O ratio of pregnant and spent streams, not by pH alone. For gibbsitic bauxite processed at 140–160 °C, free NaOH in the digester is maintained at 120–180 g/L Na2O; boehmitic feed is processed at 200–230 °C and diasporic feed at 240–270 °C, with free NaOH from 180 g/L to 250 g/L Na2O. The heat of solution of solid NaOH is sufficient to raise a 50% w/w mix above 90 °C under adiabatic conditions, so flake charging is staged through vented dissolving tanks with external cooling or recirculation. Pregnant liquor entering precipitation typically carries an A/C ratio of 0.60–0.70; spent liquor leaves precipitation at 0.30–0.40. Caustic losses occur through entrainment in red mud and through formation of desilication products during bauxite pre-desilication; counter-current red mud washing is targeted to a final free caustic level below 5 g/L Na2O. Low carbonate in 98% flake reduces the dead load sent to the recausticizing circuit, where sodium carbonate would otherwise require conversion with slaked lime.

    Bayer liquor parameterGibbsitic bauxiteBoehmiteDiaspore
    Digestion temperature (°C)140–160200–230240–270
    Free NaOH (g/L Na2O)120–180180–250200–250
    Pregnant A/C ratio0.60–0.70
    Spent A/C ratio0.30–0.40

    Production-scale single-stream autoclaves with shell-and-tube heat exchangers are sensitive to local caustic concentration spikes. High-density caustic pockets increase liquor viscosity and lower heat-transfer coefficient; if digester caustic exceeds 250 g/L Na2O, sodium aluminosilicate scale formation accelerates on heater tube surfaces. Make-up flake is therefore metered into the spent liquor return header at a controlled rate of dissolution, not into the bauxite slurry inlet. This arrangement limits localized supersaturation and protects downstream precipitation seed surfaces from residual undissolved NaOH particles.

    How Does White Liquor Charge Affect Kappa Number and Pulp Yield?

    White liquor in kraft pulping is a mixture of sodium hydroxide and sodium sulfide. Effective alkali is defined as NaOH plus one-half Na2S, both expressed as Na2O, and active alkali is NaOH plus all Na2S. For bleachable softwood kraft, effective alkali charges of 15–25% on oven-dry wood with sulfidity of 25–35% are common; hardwood pulping typically runs at 12–20% effective alkali. Raising effective alkali accelerates delignification but also increases carbohydrate degradation through peeling reactions and secondary dissolution. At constant H-factor, kappa number per TAPPI T236 cm-85 falls as effective alkali increases; a bleachable softwood kappa target of 25–32 is typical, while linerboard may be cooked to kappa 60–100. Yield at bleachable kappa is approximately 45–50%, rising to 55–65% for high-kappa grades.

    98% flake is dissolved to maintain white liquor effective alkali after recirculation. In continuous digesters with a liquor-to-wood ratio of 3.5–4.5:1, residual effective alkali at the blow line is typically held above 5–8 g/L Na2O; lower values risk lignin reprecipitation and blow-line fouling. Sodium carbonate introduced with lower-grade caustic does not contribute to delignification and instead loads the lime kiln recausticizing loop. A Na2CO3 specification below 0.8% is therefore operationally significant for mills with tight chemical recovery.

    Caustic Soda Concentration Windows for Cellulose Swelling

    Mercerization of cotton textiles with 98% flake-derived NaOH operates within a narrow concentration band of 18–24% w/w at 15–25 °C. Below 12%, sodium hydroxide swells cellulose but does not convert native cellulose I to sodium cellulose I; after washing, mercerized cellulose II develops only when the caustic concentration enters the 18–24% window. Fabric is processed on chain mercerizing machines under controlled warp tension for woven goods, while knit mercerizing machines handle tubular or open-width knits with lower tension. Impregnation is followed by hot-wash recovery at 70–90 °C to strip NaOH from the swollen fiber. Wash liquor at 5–10% NaOH is concentrated by evaporation for reuse. Low chloride content in 98% flake reduces pitting risk in stainless steel recovery evaporators and prevents localized fiber damage during high-temperature washing.

    Terminal products include mercerized cotton shirting, embroidery thread, and dimensionally stable knitwear. Dye uptake improvement is evaluated by controlled reactive or direct dyeing trials; the effect is process-dependent because tension, residence time, and caustic removal rate shift the cellulose crystallinity profile. A 98% assay flake allows preparation of mercerizing baths without the higher sodium carbonate carryover that reduces effective alkali and slows wetting.

    Saponification of palm or coconut triglycerides with flake caustic soda proceeds via three-step base-catalyzed acyl cleavage, consuming 3 mol NaOH per 1 mol triglyceride. For a vegetable oil with saponification value measured per ISO 3657:2023, the stoichiometric NaOH charge equals SV × 40.00/56.11/1000 grams NaOH per gram oil. A palm oil with SV 190–203 mg KOH/g therefore requires 0.135–0.145 g NaOH/g oil; coconut oil with SV 248–265 mg KOH/g requires 0.177–0.189 g NaOH/g oil. In industrial batch kettles at 80–100 °C, 98% flake is pre-dissolved to 30–50% NaOH and dosed into the oil phase over 30–60 min under high-shear agitation to prevent localized gelation.

    Excess NaOH is maintained at 0.5–1.0% over the calculated stoichiometric charge to drive saponification to completion; finished soap free alkali is adjusted below 0.1% as NaOH. For high free fatty acid crude oils, caustic refining before saponification generates soapstock and requires additional NaOH based on acid value; excessive free alkali in the centrifuge feed thickens the emulsion layer and reduces separation efficiency. Spent lye containing glycerol is evaporated and purified. Low carbonate in 98% flake limits ash contamination in recovered crude glycerine and avoids foaming in the saponification kettle.

    When pH Adjustment Must Meet AWWA B501 Limits

    In drinking water treatment, sodium hydroxide is selected over lime or soda ash when the objective is to raise finished-water pH without adding carbonate alkalinity or calcium hardness. Dosing is determined by raw-water buffer intensity and is controlled by a pH trim loop at the clearwell inlet, typically targeting 7.8–8.5 for distribution-system corrosion control. In softening plants, caustic is used to maintain basin pH at 9.5–10.5. The chemical must conform to AWWA B501-19 and be certified under NSF/ANSI/CAN 60 for potable use. 98% flake is dissolved on site to 0.5–2.0% w/w NaOH solution; metering pumps are trimmed against downstream pH analyzers with response times shorter than the clearwell detention time.

    Standard designationScopeRelevant control parameter for 98% flakes
    AWWA B501-19Sodium hydroxide for potable water treatmentNaOH assay, NaCl, Fe, heavy metals
    NSF/ANSI/CAN 60Drinking water treatment chemicals health effectsTrace metal and radionuclide limits
    EN 896:2012Sodium hydroxide for water intended for human consumptionPurity, insoluble matter, Fe, heavy metals
    GB 209-2006Industrial sodium hydroxide, ChinaNaOH assay, Na2CO3, NaCl, Fe for solid grades

    Operational boundary: a 50% w/w NaOH solution has a freezing point near 12 °C; outdoor storage in cold climates requires heat tracing. Solid flake addition into plant water must be staged, and water should never be added directly onto a hopper containing concentrated flake because the resulting localized temperature rise can generate violent boiling and caustic mist.

    Excess Caustic Control in Continuous Hypochlorite Reactors

    Sodium hypochlorite generation from chlorine gas and caustic soda consumes 2 mol NaOH per 1 mol Cl2. Per kg chlorine, the stoichiometric NaOH demand is 1.128 kg, derived from the molecular weight ratio 80.00/70.91. In continuous production, 98% flake is dissolved to 20–25% NaOH and fed to a packed tower or venturi contactor. Chlorine absorption is highly exothermic; chilled-water or brine heat exchangers keep the reactor outlet below 30 °C because chlorate formation via hypochlorite disproportionation accelerates with temperature. Residual excess NaOH is held at 0.2–0.5% w/w in the finished bleach to suppress hypochlorous acid formation and slow decomposition. Transition-metal contamination, especially iron above 1 mg/kg, catalyses oxygen evolution and reduces sodium hypochlorite shelf life; low iron in 98% flake is therefore a critical purchasing specification. Final bleach is filtered and tested against AWWA B300-18 for sodium hypochlorite.

    Reactor wetted parts are specified in titanium, Hastelloy C, or PTFE-lined steel because hypochlorite with free caustic attacks unprotected stainless. Caustic feed must be free of undissolved flakes; a 10–20 µm in-line filter protects the venturi nozzle from plugging. Chlorine flow is ratio-controlled to caustic flow with a feed-forward pH correction: a drop in excess NaOH below 0.1% shifts the equilibrium toward hypochlorous acid, which decomposes faster and reduces oxidation capacity.

    Water-based drilling fluids consume sodium hydroxide in small continuous doses to maintain alkaline pH, control divalent ion solubility, and preserve the performance of lignosulfonate or polyanionic cellulose deflocculants. The target pH window is commonly 9.5–10.5 for lignosulfonate muds, measured per API 13B-1:2017. In high-hardness make-up water, NaOH addition precipitates magnesium and calcium hydroxides; pushing pH above 12 removes Ca²⁺ but can alter bentonite hydration and gel structure. HPHT wells with CO2 or H2S influx require incremental caustic additions based on filtrate alkalinity tests, not bulk pH alone. 98% flake is mixed into pre-hydrated bentonite systems through a chemical dosing hopper at a controlled rate; localized high-pH zones can break down polymer viscosifiers before dispersion.

    At low concentrations, caustic also extends the gel strength of bentone-based drilling fluids by maintaining sodium ion activity; overdosing produces brittle gel structures and increases fluid-loss values. Dosing is therefore trimmed to a narrow pH range rather than to a single setpoint, and field engineers track Pm and Pf alkalinity data from API 13B-1 filtrate measurements to anticipate carbonate/bicarbonate buffering shifts.

    What Limits Caustic Soda Dosage in CIP Sequences?

    In clean-in-place cleaning of dairy, beverage, and pharmaceutical process lines, sodium hydroxide hydrolyzes protein films and saponifies fat residues. A typical caustic wash circulates at 1.0–2.5% w/w NaOH at 70–85 °C for 15–45 min, with flow velocity in stainless steel pipes held at 1.5–2.1 m/s to generate turbulent shear. Concentration above 3.0% does not proportionally improve soil removal and increases stress corrosion cracking risk in stainless steel when chlorides are present. Conductivity setpoints are calibrated by titration against actual NaOH strength because temperature, soil load, and rinse-water mineral content shift baseline conductivity. Caustic wash is followed by an acid rinse, typically nitric or phosphoric, to neutralize residual alkali and remove mineral scale, preventing protein redeposition.

    For cold-clean applications below 50 °C, caustic concentration is raised to 3.0–4.0% and soaking time is extended, but energy and chemical cost rise sharply. 98% flake with low chloride is preferred for stainless steel systems because chloride accelerates pitting and stress corrosion when combined with caustic at elevated temperature. Spent CIP solutions are membrane-filtered to extend bath life; the soil load is measured by turbidity or chemical oxygen demand, and fresh 98% flake is charged only when titrated NaOH drops below the target.

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    Certification & Compliance
    More Introduction

    Sodium hydroxide caustic soda flakes 98% manufactured in China are white deliquescent platelets of sodium hydroxide with a minimum assay of 98.0% by mass on an as-received basis. The material is identified by CAS 1310-73-2, classified for transport as UN 1823, and commonly cleared under import code 28151100. The active component is NaOH, with a molecular weight of 39.997 g/mol, a crystalline density near 2.13 g/cm³, and a melting point of approximately 318 °C. The industrial designation “98% flakes” indicates that sodium hydroxide constitutes at least 98.0% of the mass, while sodium carbonate, sodium chloride, iron oxide, and sulfate account for the balance. Flake geometry is produced by solidifying a concentrated sodium hydroxide melt on a cooled drum, yielding irregular platelets commonly 1–5 mm thick and 5–20 mm across. The material is hygroscopic and deliquescent; exposure to ambient moisture and carbon dioxide forms a surface brine film and sodium carbonate crust that can lead to caking and loss of free-flowing character. Standard export packaging includes 25 kg woven polypropylene bags with inner polyethylene liners and 1 t or 1.25 t flexible intermediate bulk containers.

    Commercial model designation is not uniform across manufacturers. The product is typically labelled as “caustic soda flakes 98% min,” “NaOH flakes 98%,” or “industrial grade I” with reference to GB/T 209-2018. Buyers should confirm the actual certificate of analysis because the model name alone does not define the chloride, carbonate, or iron content for a specific shipment.

    What Processing Differences Exist Between Flake, Pearl, and Liquid Sodium Hydroxide?

    Flake morphology presents a lower surface area-to-mass ratio than pearl or prill material of the same chemical purity. During dissolution in an agitated tank, the flake particle wets more slowly than a pearl because the platelet shape reduces the solid–liquid interface available for water penetration. The practical consequence is a longer batch cycle unless the flakes are fed through a lump breaker or wetting cone directly into the impeller zone. Flakes generate fewer airborne respirable fines than granular or powdered caustic soda, but bag emptying can still release dust and requires local exhaust ventilation or a dust-tight tipping station. Liquid sodium hydroxide at 50% mass fraction eliminates the dissolution step and is preferred in continuous dosing loops where consistent concentration is required. The liquid product, however, has a freezing point near 12 °C, which necessitates heated storage tanks, trace lines, and insulated piping in cold environments.

    ParameterFlakes 98%Pearls 98%Liquid 50%
    NaOH mass fraction≥98.0%≥98.0%≥50.0%
    Bulk density1.1–1.3 kg/L1.2–1.4 kg/L1.53 kg/L at 20 °C
    Dissolution behaviourModerate exotherm; slower wetting; requires agitationFaster wetting; free-flowing; requires agitationNot applicable; direct dosing
    Dust generationLow to moderate during bag emptyingLowNone
    Storage freeze riskSolid; caking if moisture absorbedSolid; caking if moisture absorbedFreezes near 12 °C

    The choice between flake and pearl is frequently driven by silo handling, metering accuracy, and bag residual loss. Pearls are generally free-flowing and bridge less frequently in conical silo hoppers; flakes may require a bin activator or vibratory discharge because interlocked platelets can form stable arches. Flake material, however, is more widely available in some export markets and is often priced below pearl-grade material for bulk neutralization and alkaline cleaning formulations.

    Typical certificate-of-analysis limits for Chinese 98% flake are aligned to GB/T 209-2018, industrial sodium hydroxide, solid grade I. Total alkalinity is reported as NaOH, and the impurity profile is limited as follows.

    ParameterTypical limitAnalytical approach
    NaOH mass fraction≥98.0%Acid-base titration; ASTM E291-18 or GB/T 209-2018
    Na2CO3≤0.8%Acidimetric after barium chloride precipitation or vendor method
    NaCl≤0.05%Potentiometric titration or turbidimetry
    Fe2O3≤0.005%Spectrophotometric, 1,10-phenanthroline complexation
    Na2SO4≤0.03%Ion chromatography or gravimetric barium sulfate

    Instead of relying solely on a certificate of analysis, a laboratory controlling incoming flake quality should determine total alkalinity by acid-base titration under CO2-free conditions because atmospheric carbon dioxide neutralizes dissolved NaOH and biases the free alkalinity result. The total alkalinity method in ASTM E291-18 is frequently used in import inspection, while GB/T 209-2018 remains the reference specification for Chinese domestic grade classification. Sampling should follow a recognized bulk solids scheme; the sample should be sealed immediately after collection and protected from humidity. When the flake is dissolved for quality control, the resulting solution should be filtered through a 0.45 µm membrane if turbidity from undissolved carbonate or silicate is present, because suspended solids interfere with spectrophotometric iron determination.

    Batch-to-batch variability in 98% flake shipments from different Chinese manufacturers tends to appear in sodium carbonate and iron oxide values rather than in total alkalinity. Facilities that receive containers from multiple suppliers should compare certificates against the same GB/T 209-2018 grade designation and retain a sample from each lot. In high-volume alkaline cleaning compound production, flake from a single supplier may show lot-to-lot deviations in bulk density of approximately ±0.05 kg/L; such variation does not affect chemical assay but can alter volumetric feeder calibration on a twin-screw compounding line. The feeder should be calibrated with the actual flake lot rather than with a dry free-flowing reference material because interlocked flake particles and surface moisture change the fill factor of the feed screw.

    When the Heat of Solution Is Released Into a Jacketed Dissolving Skid

    Dissolution of solid NaOH in water is strongly exothermic. The integral heat of solution at infinite dilution is approximately −44.5 kJ/mol. In a batch dissolving system, uncontrolled flake addition can raise the liquid temperature above the atmospheric boiling point, generating steam and caustic aerosol. A standard industrial skid therefore consists of a jacketed or limpet-coil vessel, a retreat-curve impeller or axial-flow turbine, a rotary valve or screw feeder for flake addition, and a temperature interlock that stops the feeder when the solution exceeds 70–80 °C. Water is always charged first and agitation is run before solid addition begins. The 98% flake should be added into the vortex at a rate that maintains the batch below the specified maximum; for a 20,000 L vessel producing 50% NaOH, the cooling duty can exceed 1.0 MW during peak addition rates, although published data for this specific vessel size is limited and vendor-specific heat transfer calculations are required.

    In continuous neutralization, a flake-derived 50% NaOH solution is metered by a positive displacement pump into a recirculating acidic stream. The injection point is followed by a static mixer, and the recirculation loop returns a slipstream to the metering pump suction to reduce concentration gradients. A temperature element downstream of the static mixer is interlocked with the alkali pump; if the mixed-stream temperature exceeds 60 °C because of acid–base neutralization heat, the alkali pump stops and the acid feed remains open. This control prevents localized boiling, vapor-phase corrosion, and deposition of sodium salts in the injection quill. The quill is fabricated from PTFE-lined carbon steel or a suitable nickel alloy because the wetting zone experiences alternating acidic and alkaline conditions. Sodium hydroxide solutions react with carbon dioxide from air or wastewater to form sodium carbonate; in hard-water neutralization, calcium carbonate scaling on the static mixer can occur when the local pH exceeds 10.0. The dosing skid is therefore flushed with soft water after each batch to prevent carbonate scale accumulation.

    In alumina refineries, 98% flake is dissolved with recycled spent liquor to produce Bayer digestion liquor. Low-temperature digestion of gibbsitic bauxite is typically carried out at 140–150 °C with caustic concentrations in the range 140–160 g/L Na2O, while boehmitic ores may require 200–250 °C and higher caustic loadings. The flake product’s low iron oxide specification contributes to controlling iron contamination in the alumina product, although refinery-grade Bayer liquor is also managed through filtration and precipitation steps. In kraft pulp mills, the flakes are mixed with sodium sulfide and sodium carbonate in the recausticizing area to produce white liquor. Cooking of softwood or hardwood chips is normally performed with effective alkali charges of 15–25% on oven-dry wood and cooking temperatures of 150–170 °C. The chloride content of the flake can concentrate in the recovery cycle; a limit near ≤0.05% NaCl is generally acceptable for many mills, but bleach plants and closed-cycle mills may require tighter chloride control. Textile mercerization uses NaOH in the 18–25 °Bé range at 15–25 °C. Flake-derived mercerizing liquor is filtered or settled before contact with cotton because undissolved carbonate particles and iron-bearing fines can deposit on the fabric and reduce luster uniformity.

    Storage, Moisture Uptake, and Corrosion Boundaries

    Sodium hydroxide flakes 98% should be stored in a dry, covered area with floor containment. The solid absorbs water and CO2 from air; partially emptied bags should be folded and secured to minimize the formation of a sodium carbonate crust. Aluminum, magnesium, zinc, tin, and galvanized steel are incompatible with sodium hydroxide solutions because the metal is attacked with evolution of hydrogen. Concentrated NaOH service at ambient temperatures commonly uses carbon steel tanks and piping, but carbon steel may require stress-relief and careful control at temperatures above 60 °C because of caustic stress corrosion cracking risk in some conditions. For pumps, seals, and small-bore lines, PTFE-lined steel, polypropylene, or a high-nickel alloy is used depending on temperature and concentration. The product does not burn, but its heat of solution can raise the temperature of wet paper, wood, or other organic material to ignition in a confined and wetted bulk spill. For this reason, spills should be recovered dry with a polypropylene shovel or vacuum system and placed into a closable caustic-resistant container. Water flushing of large spills is appropriate only with pH neutralization and drain control; uncontrolled flushing can release high-pH water that violates discharge limits for aquatic systems.

    Occupational exposure to caustic soda is controlled by containment and personal protective equipment. The NIOSH IDLH for sodium hydroxide is 10 mg/m³. Eye protection should meet ANSI Z87.1 or equivalent splash goggle standards, and protective gloves should be tested against alkali permeation under EN 374. Contaminated clothing should be removed immediately and affected skin flushed with water for at least 15 min. Emergency showers and eyewash stations should be located within 10 s travel of a bag dumping station or dissolving skid.

    Compared with 96% sodium hydroxide flakes, the 98% grade carries lower sodium carbonate and sodium chloride loads. This difference matters in closed-loop pulping liquors where chloride accumulation accelerates corrosion, and in organic synthesis where iron oxide can shorten catalyst life or darken product color. Compared with 99% flakes produced from membrane-cell feedstock, the 98% grade is typically used in bulk neutralization, extraction, cleaning, and process pH control where the extra cost of a lower-chloride specification is not justified. The 98% industrial flake is not automatically food-grade or pharmaceutical-grade; FCC and USP monographs impose separate limits on heavy metals, mercury, and chloride that a generic industrial certificate may not address. For alkyd resin catalysts, epoxide ring-opening reactions, or trace metal-sensitive polymerization systems, a 99% grade or liquid membrane-cell caustic soda should be specified after reviewing the actual chloride and iron certificate values. The product also differs from liquid 50% caustic soda in transport and unloading: solid flake reduces freight mass but requires on-site dissolution, while liquid caustic reduces labor and exposure risk but increases heated storage and freeze-protection requirements.