| HS Code | 530368 |
| Product Name | Caustic Soda Prills Price Per Ton |
| Product Type | Industrial chemical |
| Chemical Formula | NaOH |
| Cas Number | 1310-73-2 |
| Appearance | White spherical prills |
| Purity | 99% minimum |
| Price Per Ton | USD 450-550 per metric ton |
| Price Basis | FOB/CIF depending on destination |
| Packaging | 25kg PP woven bags or 50kg bags |
| Mesh Size | 2-4 mm typical |
| Solubility | Readily soluble in water |
| Production Method | Chloralkali process |
| Hs Code | 2815.11 |
| Typical Application | Soap, paper, textile, water treatment |
As an accredited Caustic Soda Prills Price Per Ton factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaging: 25kg multi-layer PP bags, 40 bags per pallet, total 1,000kg, shrink-wrapped and labeled. |
| Container Loading (20′ FCL) | 20′ FCL loads caustic soda prills in 25kg bags, palletized, max ~20–22 tons, priced per ton. |
| Shipping | Caustic soda prills ship in sealed 25kg bags, jumbo bags, or drums, palletized and wrapped. Transport via truck, rail, or container vessel. As a corrosive alkali (UN1823, Class 8), strict hazard labeling, segregation from acids/moisture, and dry, ventilated conditions are required. |
| Storage | Caustic soda prills must be stored in a cool, dry, well-ventilated area inside sealed, moisture-proof containers to prevent caking and degradation. Keep off the ground on pallets and away from acids, aluminum, and reactive metals. Ensure containers are clearly labeled, with spill containment available. Use appropriate PPE during handling to avoid chemical burns. |
| Shelf Life | Stable for years if stored sealed in dry, cool conditions; absorbs moisture and CO2, reducing purity over time. |
Procurement of sodium hydroxide prills on a per-ton basis requires specification of dry assay, particle size, packaging class, and application use rate. All addition ratios in the scenarios below are expressed on a 100% NaOH basis except where a solution strength is stated directly. Per-ton pricing is influenced by UN 1823 Class 8 transport packaging, moisture protection, residual carbonate formation during storage, and the purity grade purchased; these variables are independent of downstream chemistry.
| Downstream application | Standard designation | Controlled parameter |
|---|---|---|
| Water-based drilling fluid | ISO 10414-1:2008 / API RP 13B-1 | pH, methylene blue capacity, filtrate alkalinity |
| Kraft white liquor | TAPPI T 624 cm-11 | Active alkali in white and green liquors |
| Soap saponification | AOCS Da 16-48 / ISO 456:2001 | Saponification value; free caustic alkali |
| Sodium hypochlorite | ANSI/AWWA B300-18 | Available chlorine, excess alkali, trace metals |
| Biodiesel | EN 14214:2012+A2:2019 / ASTM D6751-23 | Acid number, total contamination, oxidation stability |
| Food-grade lye peeling | FDA 21 CFR 184.1763 / FCC monograph | GRAS status, heavy metal and arsenic limits |
In water-based drilling fluid formulation, sodium hydroxide prills are dissolved in a dedicated chemical barrel with a centrifugal agitator before introduction into the active mud system. Dry prills fed directly through a high-shear hopper generate local pH spikes above 12.0 that flocculate bentonite, reduce plastic viscosity, and produce screen blinding on the shale shaker. The target pH range for dispersed and non-dispersed water-based muds lies between 9.5 and 11.0, with a typical addition rate of 0.25 to 2.0 kg/m³, adjusted for produced-water hardness, carbonate alkalinity, and drilled formation salinity. The addition point is usually in the active mud pit after mechanical solids-control equipment, allowing hydroxide to precipitate calcium and magnesium as insoluble hydroxides before the fluid is pumped downhole. Field testing follows ISO 10414-1:2008 / API RP 13B-1 for pH, methylene blue capacity, and filtrate alkalinity. The terminal product is a water-based drilling fluid system used for cuttings transport, wellbore stability, and formation pressure control in oil and gas drilling operations.
The kraft pulping recovery cycle uses sodium hydroxide prills as the sodium make-up stream for white liquor after recausticizing losses. Make-up prills are dissolved into weak wash liquor and transferred to the recausticizing circuit, which includes a lime slaker, three-compartment causticizers, and a white liquor clarifier. The effective alkali charge for bleached softwood kraft pulp is typically 14% to 20% on oven-dry wood; bleachable hardwood charges are commonly 12% to 18%, with the lower values applied to fast-cooking eucalyptus and higher values to slow-cooking softwood. Continuous digesters operate at 150°C to 170°C for 6 to 10 hours, followed by blow-tank depressurisation, brown-stock washing, and oxygen delignification. Liquor composition is verified by TAPPI T 624 cm-11 for white and green liquor active alkali; residual active alkali is maintained in the blow line above 8 g/L to 12 g/L to prevent lignin re-deposition on fibre surfaces. A persistent bottleneck in mill operations is calcium carryover from the white liquor clarifier exceeding 50 mg/L, which scales digester screens and plugs extraction screens. The terminal finished product is either unbleached or bleached kraft pulp used in linerboard, sack paper, and printing and writing grades.
For sodium-based batch soap manufacture, the caustic soda dosage is calculated from the saponification value of the oil blend rather than set as a fixed formula ratio. The required NaOH, in g per 100 g fat, equals the saponification value multiplied by 0.0713; industrial oil charges containing palm and palm kernel fractions typically demand 13.9% to 17.8% NaOH by oil mass. Sodium hydroxide prills are dissolved to a 25–30 wt% aqueous solution and added to a steam-jacketed kettle operating at 80°C to 100°C under high-shear paddle agitation, with saponification completed in 2 to 4 hours. Incoming oil is assayed according to AOCS Da 16-48; free caustic alkali in the finished soap is measured per ISO 456:2001. The finished neat soap is dried on a chill roll or spray dryer and extruded as noodles. Terminal product forms include toilet soap bars, laundry soap sheets, and glycerin-containing soap chips. Free alkali in the finished bar is held below 0.05% to control bar cracking and consumer skin pH drift; excess hydroxide above 2 wt% in the saponification charge is avoided because it produces brittle bars and increases free caustic alkali in the finished chip.
Sodium hypochlorite production from caustic prills requires a cooled reaction loop in which 12–14 wt% sodium hydroxide solution is sparged with chlorine gas in a packed tower or venturi contactor. The stoichiometric consumption is 1.075 kg NaOH per 1 kg NaOCl generated; commercial bleach at 10–15% available chlorine typically retains 0.3–1.0 wt% excess hydroxide to stabilise the final solution and suppress chlorate formation. Reaction temperature is controlled between 10°C and 30°C through a shell-and-tube heat exchanger, and transition-metal contamination from iron, nickel, or copper is kept below trace levels because these species catalytically decompose hypochlorite and release oxygen gas. Compliance with ANSI/AWWA B300-18 governs available chlorine content, excess alkali, and trace metal limits for municipal and industrial disinfection. The terminal product is sodium hypochlorite solution used in drinking water treatment, wastewater disinfection, and household bleach.
In sodium-hydroxide-catalysed transesterification, refined vegetable oil with an acid value below 0.5 mg KOH/g and moisture below 0.05 wt% is converted to fatty acid methyl esters using a methoxide solution prepared from 0.5% to 1.5% NaOH relative to oil mass dissolved in anhydrous methanol at a 25–35 wt% concentration. The methoxide is injected into a continuous stirred-tank reactor or in-line high-shear mixer at 50°C to 65°C, followed by gravity settling or centrifugal separation of glycerin and ester phases. The finished ester is washed or dry-purified to meet EN 14214:2012+A2:2019 / ASTM D6751-23 limits for acid number, total contamination, and oxidation stability. Terminal products are B100 fatty acid methyl esters or blendstock for diesel fuel. When the feedstock free fatty acid value exceeds 5 mg KOH/g, direct caustic methoxide addition generates excessive soap and emulsifies the glycerin phase; plant configurations therefore place an acid esterification unit upstream before caustic catalysis.
Food-grade lye peeling uses 8–15 wt% NaOH solution at 60–90°C for 30 seconds to 5 minutes under FDA 21 CFR 184.1763 and FCC monograph purity limits; the solution hydrolyses pectin on tomatoes and potatoes before a rotary drum washer with acidified rinse neutralises residual alkali for canned tomato, frozen french fry, peach, and potato chip finished products.
Competitive Caustic Soda Prills Price Per Ton prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Caustic Soda Prills Price Per Ton is the commercial specification value for solid sodium hydroxide supplied as white spherical micropearls under CAS 1310-73-2, UN 1823, and EC 215-185-5. The product is procured on a dry NaOH basis, with a typical assay of not less than 99.0 wt% determined by ASTM E291-18 acid-base titration. Representative bulk properties include a particle-size band of 0.5 mm to 1.2 mm, pour bulk density between 1.10 g/cm³ and 1.28 g/cm³, and a heat of solution of approximately −44.5 kJ/mol at infinite dilution. The material is packed in 25 kg woven bags, 50 kg drums, or 1000 kg flexible intermediate bulk containers, and the price per ton is quoted as FOB production site, CIF destination port, or delivered to works with freight and packaging shown as separately invoiced line items. A representative grade designation such as CSP-99/0.5-0.1 identifies 99.0 wt% NaOH, 0.5 wt% maximum Na₂CO₃, and 0.1 wt% maximum NaCl.
| Parameter | Test method | Typical limit or range |
|---|---|---|
| Appearance | Visual inspection | White spherical prills, no lumps |
| NaOH assay | ASTM E291-18 | ≥ 99.0 wt% |
| Na₂CO₃ | ISO 3196:1975 | ≤ 0.5 wt% |
| NaCl | ASTM E291-18 | ≤ 0.1 wt% |
| Fe₂O₃ | ASTM E291-18 photometric | ≤ 0.002 wt% |
| Na₂SO₄ | ASTM E291-18 | ≤ 0.02 wt% |
| Particle size retained on 1.0 mm | ISO 565 | ≤ 2.0 wt% |
| Particle size passing 0.15 mm | ISO 565 | ≤ 10.0 wt% |
| Pour bulk density | 1 L graduated cylinder, untapped | 1.10–1.28 g/cm³ |
Low-iron grades with Fe₂O₃ ≤ 0.002 wt% are specified in rayon spin-bath make-up and synthetic detergent granulation where transition-metal contamination triggers oxidative degradation or discoloration. Sodium carbonate at or below 0.5 wt% prevents excess buffering of mercerizing solutions; chloride above 0.1 wt% may promote pitting corrosion on 316L stainless steel transfer piping when residual caustic films are wetted by condensation under insulation. The assay and impurity profile therefore segment the product price independently of freight, because lower carbonate and chloride limits require membrane-cell caustic feedstock and additional evaporation or purification control.
Solid prill pricing is rarely a single bulk value. A purchaser buying 99.0 wt% solid is paying for 0.99 tonne of NaOH per tonne of product, whereas 50.0 wt% membrane-grade liquor contains 0.50 tonne of NaOH per tonne of product. The dry-NaOH unit price is obtained by dividing the delivered product price by the NaOH mass fraction. The freight burden for water in 50% liquor is approximately 49.5 kg of water per 100 kg of dry NaOH equivalent, which must be offset by lower raw-material cost or terminal proximity. Conversely, solid prills avoid shipping liquid water but require bagging or polypropylene liners, palletisation, and climate-controlled warehouses to prevent deliquescence. A delivered price per ton therefore contains the mill netback, the solidification premium, the packaging differential, and destination freight. Price quotations that appear inexpensive on a product-weight basis may be uneconomical when evaluated on a dry-NaOH basis with discharge, storage, and melting labour included.
In alumina refineries, caustic soda prills are fed to the Bayer circuit as a high-assay solid for inventory trim when evaporator capacity or white liquor make-up is constrained. Bauxite digestion consumes NaOH through gibbsite dissolution and boehmite attack, and the soda-lime circuit regenerates NaOH by causticizing sodium carbonate with slaked lime. Dosing prills directly into causticized green liquor can create localized exotherms if addition outpaces recirculation mixing. Standard practice is to pre-dissolve prills in a dedicated dissolving tank with forced agitation at 55 °C to 70 °C before transfer to the Bayer stream. Pre-dissolution also reduces transient aluminium hydroxide nucleation on undissolved prill surfaces, which can otherwise contribute to scale in the liquor flash tanks.
Because sodium hydroxide prills are deliquescent, storage and transfer define usable shelf life. At relative humidity above approximately 50%, surface moisture absorption increases sharply, and atmospheric CO₂ converts a thin film of NaOH to Na₂CO₃. The resulting surface carbonate forms crusts on hopper walls and reduces flow through rotary feeders. A dry-air purge of 0.5 m³/h to 2.0 m³/h per storage silo is typically used when ambient dew point exceeds 10 °C. Pneumatic transfer is preferred over screw conveying because the prills are hard but brittle; dense-phase systems with conveying velocities of 4 m/s to 8 m/s reduce pellet fracture and dust generation compared with dilute-phase systems. Fracture and attrition below 0.15 mm increase dust loading in charging hoppers, and sodium hydroxide dust is corrosive to carbon steel aspiration ducting, requiring either 316L stainless steel or humidity-controlled baghouse internals.
In textile mercerization, the prills are dissolved to a caustic concentration of 20 °Bé to 30 °Bé, corresponding to approximately 180 g/L to 300 g/L NaOH. Carbonate in the dissolving water and recirculated bath is controlled below 1.0 wt% Na₂CO₃ because carbonate softens the mercerizing action and precipitates as white deposits on tension rollers. Continuous bath reconstitution from solid prills permits tighter caustic mass-balance control than direct purchase of 50% liquor, provided the dissolution system includes a plate heat exchanger capable of removing the −44.5 kJ/mol heat of solution. If the chiller undersizes the exotherm, the bath temperature rises above the 20 °C target and reduces the swelling-induced crystallinity change in cotton.
Mercury-cell caustic historically supplied high-purity 50% liquor with low chloride and low chlorate, but residual mercury content may make it unsuitable for applications where wastewater limits or food-processing cleaning systems apply. Membrane-cell caustic prills typically avoid mercury contamination and can be supplied with sodium chloride below 0.1 wt% and sodium chlorate below 10 mg/kg when the product is evaporated from high-purity membrane liquor. Sodium chlorate is not a neutral impurity in acid-gas scrubbing: it can oxidize reduced sulfur compounds and produce unwanted sulfate sludges. Buyers comparing sources should specify the mercury, nickel, and chlorate ceilings in the purchase order, not merely the NaOH assay, because standard 99.0 wt% industrial prills may carry trace levels that are incompatible with rayon, pharmaceutical, or food-contact cleaning use.
Caustic soda prills differ from flakes primarily in geometry, dusting, and flow. Flakes are irregularly shaped, thin, and break into angular fragments during mechanical feeding; prills are dense spheres with a lower surface-area-to-volume ratio for a given screen cut. The spherical geometry produces less interparticle friction and fewer fines during air conveying, but it also reduces the initial dissolution surface area relative to flakes of equivalent mass. In stirred dissolving tanks, this difference is compensated by maintaining vortex depth above half the tank diameter and by avoiding addition directly into the vortex, which can entrain air and form floating rafts of partially hydrated prills. A dissolution tank with a top-entering turbine impeller operating at a tip speed of 3.0 m/s to 4.5 m/s provides sufficient shear for the prill size range while limiting dust carryover.
In kraft pulp mills, prills are used for make-up alkali to the white liquor circuit, where NaOH is required to maintain effective alkali charge when oxidised white liquor or causticized liquor is weak. The prills are dissolved into weak wash or filtered water at 40 °C to 60 °C and then metered into the white liquor tank. Because kraft white liquor contains sodium sulfide, direct addition of solid NaOH raises the sodium-to-sulfur ratio and may temporarily shift the cooking selectivity; therefore the addition rate is matched to the digester charging schedule and verified by a 30-minute residual effective alkali test. Localized addition to the suction side of the white liquor transfer pump is avoided because the resulting exotherm can exceed 90 °C at the pump casing and cause cavitation when the impeller eye reaches the vapor pressure of water. Published data for this specific configuration is limited, so mill-specific pump suction-temperature measurements are required before switching from liquid caustic to prill make-up.