| HS Code | 531783 |
| Product Name | Diethanolisopropanolamine (DEIPA) |
| Chemical Name | N,N-Bis(2-hydroxyethyl)isopropanolamine |
| Abbreviation | DEIPA |
| Cas Number | 6712-98-7 |
| Einecs Number | 229-764-5 |
| Molecular Formula | C7H17NO3 |
| Molecular Weight | 163.22 g/mol |
| Appearance | Colorless to pale yellow transparent liquid |
| Physical State | Liquid at room temperature |
| Odor | Mild amine odor |
| Boiling Point | >200 °C |
| Flash Point | >100 °C |
| Density | 1.08-1.12 g/cm³ at 20 °C |
| Viscosity | 100-200 mPa·s at 25 °C |
| Ph | 10-12 (1% aqueous solution) |
| Water Solubility | Miscible |
| Assay | ≥85% |
As an accredited Diethanolisopropanolamine (DEIPA) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | DEIPA packaging: 200 kg net steel drums or 1,000 kg IBC totes, securely sealed for chemical transport and storage. |
| Container Loading (20′ FCL) | 20′ FCL loading: DEIPA packed in 80 × 200 kg drums, palletized, shrink-wrapped, and secured; total net weight approximately 16,000 kg. |
| Shipping | DEIPA is generally shipped as a non-hazardous, non-regulated liquid in 200 L drums, IBC totes, or ISO tanks. Keep containers clean, sealed, and labeled with product identity and SDS. Store cool, dry, ventilated, away from acids and oxidizers. Use appropriate PPE when handling. |
| Storage | Store DEIPA in a cool, dry, well-ventilated area away from heat, ignition sources, direct sunlight, acids, and oxidizers. Keep containers tightly closed, upright, and clearly labeled. Use corrosion-resistant tanks or lined steel/polyethylene drums. Prevent moisture absorption and freezing; maintain moderate temperatures. Provide secondary containment, grounding, and spill kits. Follow local regulations and manufacturer’s SDS. Do not store with incompatible materials. |
| Shelf Life | Shelf life is typically 12–24 months if kept in original sealed containers, cool, dry, and protected from direct sunlight. |
In closed-circuit Portland cement finish milling, the feed belt receives clinker, gypsum, and limestone before the two-chamber ball mill. A diluted aqueous solution of DEIPA is sprayed onto the clinker stream at a rate of 0.01 wt% to 0.05 wt% of the clinker mass. The addition point is positioned to allow distribution before the first grinding chamber. The mill operates with a dynamic separator, and the target Blaine fineness is typically 330 m²/kg to 380 m²/kg for CEM I 42.5N production. At these fineness levels, particle agglomeration and ball coating increase mill retention time and reduce separator selectivity. DEIPA adsorbs onto freshly fractured C₃S and C₂S surfaces and lowers the surface energy barrier for further size reduction. The effect is measurable only when separator rotor speed and mill ventilation are held constant. A two-chamber mill with a length/diameter ratio of 3.0–3.5 and a grinding media charge of 28% to 32% by mill volume is common in cement finish grinding. The dynamic separator rotor speed is adjusted to keep the residue on a 45 µm sieve between 5% and 9%, measured according to EN 196-6. Compliance of the processing addition is evaluated under ASTM C465 and GB/T 26748-2011. Reference mortar strength is tested according to EN 196-1.
The process operating window is narrow because clinker chemistry and sulfate carrier solubility alter the amine response. Mill outlet temperature is maintained below 115 °C to limit thermal degradation of the alkanolamine. DEIPA dosage above 0.08 wt% may produce false set or extended setting time in laboratory trials, depending on C₃A content and fineness. Natural gypsum releases sulfate more slowly than anhydrite. This difference may require a lower DEIPA feed rate. Published production data for closed-circuit ball mills with a length/diameter ratio of 3.0–3.5 show that Blaine gains are site-specific, often between 15 m²/kg and 35 m²/kg at equal production rate. Output changes vary with clinker grindability, separator speed, and grinding media charge. A mill trial should include a stable reference period of not less than 72 h before dosage adjustment because clinker mineralogy can change between kiln campaigns. The terminal product is CEM I 42.5N or CEM I 42.5R conforming to EN 197-1 when the limestone content remains within the permitted mass fraction.
When Portland-limestone cement is produced by intergrinding clinker, limestone, and gypsum, the limestone mass fraction is held at 6% to 20% for CEM II/A-L under EN 197-1. DEIPA is added at 0.02 wt% to 0.05 wt% of the total mill feed. The softer limestone phase accumulates in the fine fraction more rapidly than clinker particles. This fine limestone fraction accelerates C-S-H nucleation and participates in early hydration reactions. DEIPA modifies the particle size distribution and the adsorption of sulfate on clinker surfaces. The combined effect is evaluated in mortar strength testing according to EN 196-1. The amine is not a water-reducing agent. Its function is not replacement of the sulfate carrier. The addition rate must be calibrated to the limestone/clinker ratio because limestone has a lower grindability index and a higher specific surface contribution. The Blaine target for CEM II/A-L 42.5N is typically 380 m²/kg to 420 m²/kg. The separator air flow is increased relative to ordinary Portland cement grinding because limestone fines dominate the fine fraction. The residue on a 45 µm sieve is usually held between 6% and 12% under EN 196-6.
The interaction between DEIPA and C₃A-rich clinker is more pronounced in intergrinding than in separate grinding. If the limestone fraction is high and the clinker fraction is reduced, the effective amine concentration on clinker surfaces can become excessive even when the total feed dosage appears low. This can lead to rapid C₃A dissolution and early stiffening under sulfate-limited conditions. Mill operators using natural gypsum with slow release should reduce the initial DEIPA dosage. The terminal product is CEM II/A-L 42.5N or CEM II/A-L 42.5R. Compliance for the blended cement includes EN 197-1 and, for North American markets, ASTM C595/C595M. The main process conflict is maintaining stable separator fines. Fine limestone affects separator cut size, and amine adsorption changes particle surface charge. For this reason the laboratory mill trial must replicate full-scale separator dynamics. Published data for this specific configuration is limited.
The intergrinding of granulated blast furnace slag with clinker and sulfate carriers presents a different surface chemistry from Portland clinker grinding. Slag mass fractions in CEM III/B production are typically 66% to 80% under EN 197-1. The slag is harder than clinker and contains a glassy aluminosilicate phase with low hydraulic activity at early age. DEIPA is introduced onto the mill table or into the recirculating elevator at 0.02 wt% to 0.06 wt% of the total feed mass. The grinding circuit often uses a vertical roller mill with hot gas drying because granulated slag moisture can be 8% to 12%. The amine is not injected into the hot gas stream but is added after the drying zone to limit thermal exposure. The product target is CEM III/B 42.5N LH with a Blaine range of 400 m²/kg to 500 m²/kg. At this high fineness, particle agglomeration limits separator efficiency. DEIPA reduces coating on the mill table and rollers. The terminal product must meet the activity index requirements of EN 15167-1 at 7 days and 28 days while maintaining the sulfate resistance class.
The sulfate balance in slag cement is more fragile than in ordinary Portland cement because the clinker content is low and the slag contributes additional alumina. Excess amine dosage can accelerate C₃A dissolution and consume the available sulfate before a stable ettringite layer forms. The consequence may be early stiffening or a reduction in workability in mortar testing. Many slag grinding plants combine DEIPA with triisopropanolamine at a low ratio. Triisopropanolamine is known to complex Fe³⁺ and accelerate ferrite hydration. DEIPA contributes to dispersion and early strength. The combined blend is tested under EN 196-1 and must satisfy the minimum strength class of CEM III/B 42.5N. The granulated slag itself must comply with EN 15167-1. Mill output gains from DEIPA in slag intergrinding are less predictable than in clinker finish grinding because slag grindability varies between steel plant sources. Without a trial on the specific slag, no dosage adjustment is technically valid.
Formulated cement grinding aid blending is a separate downstream activity from cement milling. In a blending plant, DEIPA is mixed with water, diethylene glycol, and triisopropanolamine in stainless steel or high-density polyethylene tanks. The mixture is prepared at ambient temperature with low-shear agitation. The final liquid product must remain homogeneous at storage temperatures from 5 °C to 40 °C. Commercial formulations may contain DEIPA active mass fractions from 10% to 50%, but no fixed ratio is common because clinker composition, cement type, and mill circuit configuration control the formulation. The finished grinding aid is dosed at 0.05 kg/t to 0.30 kg/t of clinker at the cement plant. In this range, the effective DEIPA concentration at the mill feed is typically 0.005 wt% to 0.05 wt% by mass of clinker. These values are not performance specifications. They are starting points for mill trials.
Quality control in the blending plant follows GB/T 26748-2011 for cement grinding aids and relevant REACH and CLP requirements for alkanolamine substances. The blend must not be mixed with nitrite-containing compounds under acidic conditions. Nitrosamine formation is a recognized hazard for secondary amine impurities and must be excluded by raw material specification and storage practice. The terminal product is not a cement. It is a formulated liquid processing additive delivered to cement terminals and integrated grinding stations. Batch-to-batch variance is controlled by amine value titration and moisture analysis. Formulators must not extrapolate a mill trial from one clinker source to another without laboratory grinding tests and mortar strength verification under EN 196-1.
| Downstream segment | DEIPA feed rate by mass of feed | Primary compliance standard | Terminal product |
|---|---|---|---|
| Closed-circuit ball mill finish grinding | 0.01–0.05 wt% | ASTM C465 | CEM I 42.5N |
| Portland-limestone cement intergrinding | 0.02–0.05 wt% | EN 197-1 | CEM II/A-L 42.5N |
| Slag cement intergrinding | 0.02–0.06 wt% | EN 197-1 and EN 15167-1 | CEM III/B 42.5N LH |
| Formulated liquid grinding aid dosing | 0.05–0.30 kg/t product | GB/T 26748-2011 | Liquid grinding aid |
High-early-strength Portland cement is ground to Blaine values above 400 m²/kg and often to 450 m²/kg for CEM I 52.5N or CEM I 52.5R. The clinker is typically low in C₃A and low in alkali. DEIPA is used at the lower end of the grinding aid range, commonly 0.01 wt% to 0.03 wt% of clinker mass. At high fineness, particle agglomeration is the dominant limitation. The amine reduces coating on mill media and improves air classifier performance. However, the cement has a high specific surface and elevated reactivity. An excessive DEIPA dosage can generate measurable air entrainment and reduce early mortar strength. Mortar testing under EN 196-1 confirms that air content and setting time remain within the declared range. In North America, the product may be evaluated under ASTM C150/C150M for Type III cement performance. The mill system is usually a closed-circuit ball mill with a high-efficiency separator running at higher rotor speed than CEM I 42.5N production. The grinding media size distribution in the first chamber is shifted to smaller media to increase surface contact area. The residue on a 45 µm sieve is often maintained below 3% under EN 196-6.
The operational boundary is narrow because the fineness target is near the agglomeration threshold. A mill operator cannot increase DEIPA dosage to solve a separator efficiency problem caused by insufficient air flow or worn separator blades. The amine does not correct a mechanical classification defect. When the mill outlet temperature exceeds 115 °C, the risk of amine degradation increases and the water in the diluted solution flashes before uniform distribution. This creates intermittent coating and unstable product quality. Laboratory batch grinding trials should accompany full-scale trials because the particle size distribution of high-fineness cement is sensitive to ball charge dynamics. Published data for DEIPA in this specific high-fineness configuration is limited.
Vertical roller mill finish grinding has a different mode of size reduction from ball milling. The material bed is compressed between rollers and the grinding table. DEIPA is sprayed onto the feed at 0.01 wt% to 0.05 wt% of total feed mass, but water injection is kept low because the mill relies on dry bed stability. The integrated separator returns coarse particles to the table. The product particle size distribution is narrower than in ball mill cement. DEIPA modifies interparticle friction and reduces the vibration caused by an unstable grinding bed. The terminal product is CEM I or CEM II cement conforming to EN 197-1. The compliance of the processing addition is assessed under ASTM C465 or GB/T 26748-2011 depending on the market. The main operational boundary is moisture. Excess water from a diluted amine stream can destabilize the bed and raise mill vibration limits. The solution concentration should be controlled so that the total water addition remains below the mill's water tolerance. This tolerance is usually below 0.5% of feed moisture for finish grinding vertical roller mills.
Published data for DEIPA performance in vertical roller mill finish circuits is less extensive than for closed-circuit ball mills. The effect on specific grinding energy consumption is machine-dependent. Mill suppliers specify the acceptable vibration amplitude and the maximum water injection rate. A DEIPA feed trial should begin with the lowest intended dosage and be maintained for at least 8 h to observe bed stabilization. The terminal cement must meet the same strength and setting time requirements as ball mill cement. The selection between DEIPA and other alkanolamines depends on the cement type and the sulfate carrier. No universal conversion factor exists between ball mill and vertical roller mill dosing.
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Diethanolisopropanolamine (DEIPA) is a tertiary alkanolamine corresponding to CAS 6712-98-7 and chemical name N,N-bis(2-hydroxyethyl)isopropanolamine. The compound is produced by ethoxylation of monoisopropanolamine, yielding a molecule with one tertiary amine centre and three terminal hydroxyl groups. Its molecular formula is C₇H₁₇NO₃, and the calculated molar mass is 163.22 g/mol. Commercial DEIPA is typically supplied as a clear, colourless to pale-yellow hygroscopic liquid with an active assay of 85–90 % as determined by gas chromatography, with the balance consisting of water and low-level residual amines. The product is water-miscible, polar, and alkaline. In cement grinding aid packages, DEIPA is not a direct replacement for triethanolamine (TEA) or triisopropanolamine (TIPA); rather, it is selected as a co-formulant when controlled changes in grinding efficiency, pack-set behaviour, and mortar strength development are required. The molecule differs from methyl diethanolamine (MDEA) and monoethanolamine (MEA) in amine classification, molecular weight, and acid-gas reactivity; these differences are material to both storage design and application dosing.
Certificate-of-analysis data for bulk DEIPA are normally reported against a defined set of wet-chemical and instrumented methods. Water content is measured by coulometric Karl Fischer titration under ISO 760; colour is assessed as platinum-cobalt units under ASTM D1209-05; density is measured at 20 °C under ASTM D4052-22; refractive index is measured at 20 °C under ASTM D1218-21. Purity is typically determined by gas chromatography with flame ionisation detection, using an internal standard; published data for this specific configuration is limited. A representative bulk specification is given in Table 1. The amine value of DEIPA is frequently quoted in procurement specifications, but the number is method-dependent because non-aqueous titration of a tertiary amine must be carried out with a suitable solvent and indicator. Consequently, direct amine-value comparisons between DEIPA and primary or secondary alkanolamines without method qualifiers are not technically valid.
| Parameter | Method | Typical acceptance range |
|---|---|---|
| Appearance | Visual inspection | Clear, colourless to pale-yellow liquid |
| Purity as DEIPA | GC-FID internal standard | 85.0–90.0 % |
| Water content | ISO 760 | ≤0.5 % bulk; ≤1.0 % for some logistic modes |
| Colour | ASTM D1209-05 | ≤50 APHA |
| Density at 20 °C | ASTM D4052-22 | 1.05–1.08 g/cm³ |
| Refractive index n20/D | ASTM D1218-21 | 1.4650–1.4750 |
Because DEIPA is hygroscopic, water content can increase by more than 0.2 % in a single open-head transfer if the ambient relative humidity exceeds 60 %. For this reason, bulk storage in nitrogen-blanketed or closed-loop systems is standard for certifications requiring water content below 0.5 %. Typical packaging for DEIPA includes 200 kg high-density polyethylene drums, 1000 kg intermediate bulk containers, and bulk isotainers. For cement grinding aid producers consuming multiple daily tonnes, bulk storage is preferred because drum handling increases moisture uptake and static electricity risks during transfer. Transfer hoses should be chemical-resistant rubber or stainless-steel flex hose; natural rubber and unlined steel are not recommended for continuous exposure because the alkaline product can promote corrosion at the liquid-vapour interface. A closed-loop vapour-return line is recommended when tanker unloading is performed at ambient temperatures above 25 °C.
In closed-circuit cement milling, DEIPA is introduced either onto the clinker feed belt or through a dilute aqueous spray into the first compartment of the mill. The conventional dosage range for pure DEIPA is 0.005–0.02 wt% of cement mass. In a mill operating at 100 t/h clinker feed, a dosage of 0.01 wt% corresponds to 10 kg/h active DEIPA, or approximately 11.8 kg/h of an 85 % active commercial product. The additive is typically diluted with water to 20–40 wt% before injection through a positive-displacement metering pump; this dilution reduces localised amine concentration on hot clinker surfaces and improves dispersibility. The primary process constraint is not solution viscosity but the onset of amine adsorption onto freshly fractured clinker and calcium silicate surfaces, which changes the agglomeration state of the mill charge. Process engineers typically track mill elevator power draw, separator reject mass flow, and Blaine specific surface area against an air-permeability method. A target Blaine fineness of 3200–3800 cm²/g is common for CEM I cements under EN 197-1:2011, but the response to DEIPA is batch-dependent because clinker sulfate balance, free lime, and grinding temperature shift the adsorption equilibrium. Dosing above 0.03 wt% is generally avoided in grinding aid formulations because the resulting cement may exhibit silo flow irregularities and altered pack-set behaviour, particularly when mill outlet temperatures exceed 120 °C. Published data for this specific configuration is limited.
Clinker chemistry and mill conditions affect the response. A high free-lime clinker above 1.5 % by mass may exhibit a different adsorption isotherm for DEIPA than a low-free-lime clinker because the amine can coordinate to calcium-rich surface sites. Similarly, high sulfate clinkers may alter the competitive adsorption of sulfate ions and alkanolamines on C₃A and C₄AF surfaces. A mill trial protocol typically includes a 4-hour baseline period, an 8-hour injection period, and sample collection every 30 minutes for Blaine fineness, 45 µm sieve residue according to EN 196-6:2018, and pack-set index. Mill outlet temperature is usually kept below 120 °C to avoid thermal degradation of the amine and above the dew point to prevent pre-hydration. Inlet moisture above 2 % on clinker feed can reduce grinding aid efficiency because water competes for surface hydroxyl coordination sites. Published data for this specific configuration is limited.
In polycarboxylate ether-based concrete admixture systems, DEIPA is not used as a primary water-reducing agent. It may be present as a minor co-formulant in strength-enhancing or hydration-controlling admixtures. Compatibility is evaluated under ASTM C494/C494M-19 or EN 934-2 as appropriate to the target market, with measurement of setting time, air content, and compressive strength. At equal dosage, DEIPA does not automatically reproduce the early-age set behaviour of TEA; TEA is often associated with accelerated initial hydration at low dosage, while TIPA is more commonly associated with later-age strength effects. DEIPA occupies an intermediate position in molecular weight and hydroxyl value, and its use in commercial admixtures is typically accompanied by comparative mortar testing at 1 day, 7 days, and 28 days according to EN 196-1:2016. A dosage window of 0.005–0.02 wt% by cement mass is common in evaluation studies. Published data for this specific configuration is limited.
Air entrainment is particularly sensitive. Tertiary alkanolamines can change the surface tension of the aqueous phase, altering the bubble-size distribution produced by air-entraining admixtures. Therefore, trial batching under EN 12350-7:2019 or ASTM C231-17 should measure fresh air content and air-void spacing factor, not only compressive strength. A change of 0.5 % in air content can shift freeze-thaw durability classification; this is a critical threshold in external concrete. High C₃A cements above 8 % by mass may require lower total alkanolamine dosage because adverse setting-time changes can overshadow grinding benefits. Published data for this specific configuration is limited.
TIPA is solid at ambient temperature, with a melting point near 58 °C, and requires heated storage, trace heating, or blend dissolution before use. DEIPA remains liquid at 25 °C, which reduces the need for heated transfer lines and lowers the risk of solidification in unheated dosing cabinets. The comparative molecular and physical data are shown in Table 2. In cold-weather grinding aid formulations, DEIPA can be substituted for part or all of the TIPA fraction to maintain a pumpable, homogeneous liquid blend at temperatures below 10 °C. The substitution ratio is not a simple one-to-one replacement; formulators typically adjust the ratio between 1:3 and 3:1 DEIPA:TIPA based on mill trials. Because DEIPA has a lower calculated hydroxyl value than TEA but a higher calculated hydroxyl value than TIPA, its effect on cement paste fluidity and early hydration must be separated from the effect of the glycol carrier. The grinding aid package may include diethylene glycol, lignosulfonate, sodium acetate, or triethanolamine as secondary components. When DEIPA replaces TIPA, the viscosity of the package may decrease, and the cloud point of the aqueous blend can shift; a storage stability test at 4 °C for 7 days is therefore used to verify that no phase separation or sedimentation occurs. Published data for this specific configuration is limited.
| Property | DEIPA | TEA | TIPA |
|---|---|---|---|
| CAS Registry | 6712-98-7 | 102-71-6 | 122-20-3 |
| Molar mass | 163.22 g/mol | 149.19 g/mol | 191.27 g/mol |
| Hydroxyl groups | 3 | 3 | 3 |
| Amine type | Tertiary | Tertiary | Tertiary |
| Physical state at 25 °C | Liquid | Liquid | Solid |
| Calculated hydroxyl value | 1031 mg KOH/g | 1129 mg KOH/g | 880 mg KOH/g |
| Calculated amine value | 344 mg KOH/g | 376 mg KOH/g | 294 mg KOH/g |
Calculated hydroxyl value is not a direct measure of performance in cementitious systems; it is a structural index. DEIPA has a calculated hydroxyl value of 1031 mg KOH/g, between TEA at 1129 mg KOH/g and TIPA at 880 mg KOH/g. The calculated amine value follows the inverse order: TEA 376 mg KOH/g, DEIPA 344 mg KOH/g, and TIPA 294 mg KOH/g. These values are derived from the molar mass and functional group count, not from titration of commercial blends. Because commercial DEIPA is supplied at 85–90 % assay, a reported amine value on an as-is basis must be corrected for water content to allow comparison with pure-compound data. In procurement of closed-loop grinding aid systems, specification of DEIPA by gas-chromatographic purity is more reproducible than specification by amine value, particularly when the blend contains residual isopropanolamine and ethanolamine impurities.
DEIPA is sometimes confused with diethanolamine (DEA) because of the diethanol fragment in the commercial name. DEA is a secondary alkanolamine with a molar mass of 105.14 g/mol and is used in gas treating and chemical intermediates, whereas DEIPA is a tertiary amine with three hydroxyl groups. In gas-treating evaluations, DEIPA would be expected to have a lower acid-gas reaction rate than primary or secondary amines due to the absence of N–H protons, but published data for this specific configuration is limited. For cement applications, the tertiary structural feature is important because it avoids rapid carbamate formation and may provide a more gradual interaction with clinker surfaces.
DEIPA is hygroscopic and mildly alkaline. Bulk storage tanks are typically fabricated from 304 or 316 stainless steel, or from lined carbon steel. Nitrogen blanketing is specified when ambient relative humidity exceeds 60 % because the product can absorb water during open-head transfer. Recommended bulk storage temperature is 10–35 °C; lower temperatures increase viscosity and may require heat tracing, while higher temperatures can accelerate colour development and the formation of trace amine degradation products. The product should not be mixed with strong oxidising agents, acid chlorides, or concentrated mineral acids, because exothermic neutralisation can generate localised boiling and amine decomposition. In grinding aid formulation tanks, DEIPA is routinely blended with glycols, lignosulfonates, and other alkanolamines, but a 14-day stability test at 40 °C is typically applied to detect precipitate formation, phase separation, or viscosity drift. The material should be stored away from direct sunlight and protected from sustained exposure to air. For EU market applications, importers and formulators must verify registration status under REACH Regulation EC No 1907/2006 and provide a safety data sheet with the relevant GHS classification. No summary of the GHS classification is restated here; the safety data sheet of the specific supplier remains the controlling document.
Combination with nitrite-based corrosion inhibitors should be avoided unless the mixture is specifically assessed, because secondary amine impurities can react with nitrosating agents to form N-nitrosamines. For DEIPA, which is tertiary, the risk is lower than for secondary amines, but the presence of residual ethanolamine or isopropanolamine makes nitrite compatibility a formulation constraint. Lot-to-lot variation in DEIPA purity can affect grinding aid performance in production-scale systems. For a bulk tanker receiving 20,000 kg of 85 % DEIPA, a water content shift from 0.3 % to 0.8 % changes the active amine delivered by 100 kg per tanker. Sampling should follow a top, middle, and bottom composite procedure to account for density stratification. Retention samples are typically held at 5–15 °C for 12 months for batch-tracing investigations. Published data for this specific configuration is limited.
A workplace exposure assessment is required when DEIPA is handled in open dosing areas. The amine odour threshold is low, and vapour or mist generation during spray application should be controlled through local exhaust ventilation. Draining of transfer hoses and use of closed-loop sampling stations are common engineering controls on cement grinding aid lines. Waste water containing DEIPA should be assessed for aquatic toxicity and oxygen demand before discharge; disposal must follow national and local regulations for water-miscible alkanolamines. Spill containment capacity should be 110 % of the largest container according to local secondary containment requirements. Published data for this specific configuration is limited.