| HS Code | 937921 |
| Product Name | CELVOLIT 1318 VAE Emulsion for Polymer Cement Waterproofing Coatings |
| Polymer Type | Vinyl acetate-ethylene (VAE) copolymer emulsion |
| Appearance | Milky white liquid |
| Viscosity Mpa S | 2000-3000 |
| Ph | 4.5-6.0 |
| Particle Size Um | 0.5-2.0 |
| Residual Vinyl Acetate Percent | <0.1 |
| Film Flexibility | Flexible and tough |
| Water Resistance | Good |
| Cement Compatibility | Excellent |
As an accredited CELVOLIT 1318 VAE Emulsion for Polymer Cement Waterproofing Coatings factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in 200 kg polyethylene-lined steel drums or 1,000 kg IBC totes, sealed to prevent moisture ingress. |
| Container Loading (20′ FCL) | One 20-foot FCL container loaded with CELVOLIT 1318 VAE Emulsion, palletized, secured, and stabilized for safe polymer cement waterproofing coating transport. |
| Shipping | CELVOLIT 1318 VAE Emulsion ships as a non-hazardous water-based liquid in sealed drums, IBC totes, or bulk tankers. Protect from freezing and excessive heat; store between 5–35°C. Keep containers upright, tightly sealed, and away from direct sunlight. Ensure adequate ventilation during loading and unloading to maintain product integrity. |
| Storage | Store CELVOLIT 1318 VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area. Protect from direct sunlight, frost, and temperatures above 30°C. Ideal storage temperature is 5–30°C. Avoid contamination and freezing. Under proper conditions, shelf life is typically 6 months from manufacture date. Stir before use. |
| Shelf Life | Store in original sealed container at 5–35°C. Shelf life is 12 months from manufacture; avoid freezing. |
In interior wet-area tiling systems where the primary waterproofing barrier is bonded directly to the concrete substrate before thin-set mortar application, the liquid-applied cementitious slurry must form a continuous, pinhole-free film capable of resisting lateral moisture migration under intermittent wetting. Formulations based on CELVOLIT 1318 VAE emulsion, dosed to deliver a solid polymer-to-cement weight ratio (p/c) of 0.45–0.55, which equates to an as-supplied emulsion loading of 82–100 parts per 100 parts of cement at the nominal 55 % solids, are designed to meet the water-impermeability and adhesion requirements of EN 14891:2017 for liquid-applied water-impermeable products (type CM). The dry component typically comprises CEM I 42.5 N Portland cement, graded 0.1–0.3 mm silica sand, a retarder-modified cellulose ether, and a non-ionic defoamer; the liquid side is CELVOLIT 1318 pre-diluted with clean water to yield a total water-to-cement ratio of approximately 0.35. On site, material is processed in a forced-action mixer—commonly a Collomix Xo 1 with rotating pan and counter-current paddle—operated at 300–400 rpm for 3–4 minutes after powder addition to ensure full dispersion without entraining air. The resulting slump-free mortar, with a flow consistency of 140–160 mm as determined by the flow-table method of EN 1015-3, is transferred to the substrate and applied by notched trowel in two coats to a total dry film thickness of 1.5–2.0 mm; each coat is lightly rolled with a spiked aerator to release entrapped bubbles. Curing at ≥90 % RH for a minimum of 24 h is required prior to tile fixing. The compliance verification campaign includes the water-impermeability test under 0.2 N/mm² positive pressure for 24 h (EN 14891, clause 7.2) and the tensile adhesion strength test after 7 d water immersion (EN 14891, clause 7.5) where values must exceed 0.5 N/mm² with failure occurring cohesively within the coating layer. The finished product configuration is a two-component kit: a 25 kg sealed bag of powder and a 18 kg liquid pail, labelled for behind-tile waterproofing in bathrooms, shower enclosures, and domestic kitchens. Operating boundaries are substrate temperatures above 5 °C and ambient relative humidity below 85 % at the time of application; contact with reactive metals such as aluminium and zinc must be avoided due to alkaline hydrogen evolution. The polymer film formation, which proceeds as the cement hydrates and water is consumed, delivers the necessary flexibility and adhesion, but exposure to freezing before the mortar reaches a compressive strength of 5 N/mm² can cause irreversible film disruption and loss of waterproof integrity.
Exposed balcony decks and roof terraces subject to diurnal thermal swings greater than 40 °C and structural movement demand polymer-cement waterproofing membranes capable of bridging cracks that open and close under service conditions. CELVOLIT 1318-based formulations targeting the EN 14891:2017 crack-bridging class CB II (crack-bridging ability ≥0.75 mm at −5 °C, per clause 7.6) are adjusted to a solid polymer-to-cement weight ratio in the range 0.90–1.10, corresponding to an emulsion addition of 164–200 parts by weight per 100 parts of cement. The dry blend incorporates early-strength CEM I 52.5 N cement, graded 0.06–0.2 mm silica filler, and a small fraction of 0.5 mm maximum aggregate to limit shrinkage, while the liquid side relies on the CELVOLIT 1318 latex diluted to maintain a total w/c of 0.30–0.32. Production-scale application utilises continuous mixing pumps—such as a PFT G4 or Putzmeister MP 25 equipped with a DN 35 hose and spray gun—that blend the pre-batched liquid component with the powder, convey the slurry over distances up to 30 m, and spray a wet coat of 1.0–1.5 mm per pass. Between coats, an alkali-resistant glass fibre mesh (mesh opening 4×4 mm, weight ≥160 g/m²) is embedded to provide mechanical reinforcement against crack propagation. A total dry film thickness of 2.5–3.0 mm is built up in two or three applications; the mortar must not skin over in less than 15 minutes at 25 °C to allow proper mesh embedding. Curing proceeds for 48–72 h at >80 % RH, after which a flexible tile adhesive compliant with EN 12004 C2 S1 is installed over the membrane. Beyond crack bridging, the system is verified for tensile adhesion after freeze-thaw cycling according to EN 13687-4, requiring values above 0.5 N/mm², and for water impermeability under 0.2 N/mm² positive pressure for 7 d (EN 14891 clause 7.2). The commercial package is a two-component kit with 25 kg powder and 20 kg liquid pail, classified as a flexible waterproofing coating for exterior balconies, terraces, and walkways. Operational restrictions include a maximum substrate temperature of 30 °C during application to prevent rapid water evaporation and skinning, an interdiction to expose the uncured membrane to direct UV radiation for more than 14 d—the VAE polymer embrittles under prolonged actinic exposure—and the necessity to protect the freshly applied coat from rain for a minimum of 6 h to avoid wash-out of the unhydrated cement.
Permanent immersion in chlorinated water, with residual free chlorine concentrations maintained between 1.0 and 3.0 mg/L and pH 7.2–7.6, establishes a chemically aggressive environment that accelerates calcium hydroxide leaching and can hydrolyse ester groups in vinyl acetate copolymers if the coating is under-cured. Polymer-cement waterproofing membranes for swimming pool shells formulated with CELVOLIT 1318 operate at a solid p/c of 0.65–0.85, or an emulsion dose of 118–155 parts per 100 parts of cement, balancing low capillary porosity with sufficient polymer coalescence to resist chlorine attack. The powder fraction is built from sulfate-resisting cement (CEM I 42.5 R-SR, EN 197-1) blended with microsilica (5–7 wt% of binder) and calcined bauxite filler to mitigate sulfate-induced expansion and to densify the pore structure; the liquid component is CELVOLIT 1318 diluted to a total w/c of 0.33. Mixing is performed in a slow-speed planetary mixer for 5 minutes after the initial wetting phase, and the mortar is forced-fed into the concrete substrate pores using a sharp-edged stainless steel trowel in the first pass, followed by a flat trowel finish in the second pass to close the surface; total dry thickness is 2.0 mm. After 7 d of moist curing under wet hessian, the coating is sponge-floated to obtain a non-porous finish that minimises biofilm adhesion. Compliance with EN 1504-2:2004, principles 1.3 and 6.1, is demonstrated through water absorption <5 % per EN 1062-3, capillary water absorption <0.1 kg/(m²·h⁰·⁵) per EN 13057, and adhesion on saturated concrete ≥0.8 N/mm² per EN 1542. For drinking water contact in combined pool/tank applications, additional testing under EN 14944-1:2006 is required, with the total organic carbon migration limit set at 2.5 mg/L. The end product is supplied as a 20 kg liquid component and 25 kg powder component kit, approved for use in public and private swimming pool shells, splash-water channels, and water reservoirs. Process boundaries dictate that application be avoided when water temperature is below 10 °C; moreover, ozone-based disinfection shocks that raise dissolved ozone above 0.5 mg/L must not occur within the first 28 d of curing, as residual peroxide species can oxidise the polymer film and reduce adhesion.
Basement retaining walls accessed only from the interior impose a stringent requirement: the waterproofing membrane must resist hydrostatic pressure acting on its reverse face—negative-side water pressure—while remaining fully bonded to a substrate that is often permanently damp. CELVOLIT 1318 polymer-modified mortars employed for this service rely on a solid p/c of 0.55–0.75 (100–136 parts emulsion per 100 parts cement) to enhance adhesion under moisture-saturated conditions and to lower the modulus of the cured matrix, thereby accommodating minor substrate movements without debonding. The dry component combines rapid-hardening CEM I 52.5 R with finely ground granulated blast-furnace slag (20 % replacement) to reduce heat of hydration and minimise early shrinkage cracking. Mixing is executed in a heavy-duty paddle mixer at low speed (300 rpm) for 4 min, and the slurry must be applied within a pot life not exceeding 45 min at 20 °C. Before coating, the concrete substrate is prepared by dry grit blasting to an ICRI surface profile CSP 3; a bonding primer consisting of the liquid component diluted to p/c 0.30 and brushed in a thin film is allowed to become tacky. The main waterproofing body is then trowelled in two layers to a total dry thickness of 2.5 mm, with the first coat vigorously compacted into the profile. Curing is conducted by covering with water-saturated, non-bleeding hessian for a minimum of 5 d; any drying during this period will result in tensile adhesion values below the threshold of 0.8 N/mm² required by EN 1542 when tested after 7 d water immersion. Performance against negative hydrostatic pressure is evaluated by a modified water-penetration test following EN 12390-8: the coating, applied to a concrete slab and subjected to 0.5 N/mm² water pressure for 72 h, must restrict the penetration depth to less than 20 mm. Compliance with EN 1504-2:2004 surface protection products is mandatory, and the system is classified under principle 1.3 for water impermeability and 6.1 for resistance to moisture. The product is commercialised as a two-component kit comprising 25 kg bagged powder and 18 kg liquid, designated for interior-applied waterproofing of basement walls, lift pits, and underground car park retaining structures. Incompatibilities exist with active water-running cracks—these must be pre-injected with hydrophobic polyurethane resin—and with substrates having a moisture content above the saturated surface-dry condition, as the bonding primer cannot adequately penetrate water-filled capillaries. The coating must be protected from sub-zero temperatures for at least 72 h after application, and exposure to early hydrostatic loading before 14 d of curing can cause blistering and detachment.
Drinking water contact surfaces require a demonstrably low leaching profile governed by EN 14944-1:2006 and the European Acceptance Scheme for construction products in contact with water intended for human consumption. Cementitious waterproofing coatings for potable water storage tanks using CELVOLIT 1318 as the polymer binder are formulated at a restricted solid p/c of 0.40–0.50 (73–91 parts emulsion per 100 parts cement) to minimise the organic fraction that contributes to soluble total organic carbon (TOC) while retaining adequate water-impermeability. The powder mass comprises white Portland cement (CEM I 52.5 N, low in CrVI), and an inert limestone filler (CaCO₃ >98 %) to control the rheology and reduce the alkali background; no cellulosic thickening agents are used that could serve as nutrients for microbial growth. The liquid component is CELVOLIT 1318 diluted with deionised water to a total w/c of 0.35. The mortar is prepared in a clean stainless-steel planetary mixer with PTFE-coated paddles, mixed for 4 min, and applied by medium-stiff nylon-bristle brush in three layers to a cumulative dry film thickness of 1.5 mm. Between successive coats, a minimum 12 h curing interval at >95 % RH is observed to prevent delamination and to allow full hydration of the cement at the interface. After the final coat, curing is extended for 14 d under moist conditions before water can be stored. Conformity assessment includes the migration test for TOC (EN 14944-1, Annex B) with a pass limit of 2.5 mg/L and for specific organic substances per the positive list of the applicable national regulation. Adhesion on saturated concrete must still exceed 0.8 N/mm² per EN 1542. The terminal product is a two-component kit in 20 kg and 20 kg packaging, bearing a formal certificate of conformity for drinking water contact, and is specified for rehabilitation and new construction of concrete service reservoirs, clear water tanks, and treatment basins. Operational boundaries are critical: the carbonate-rich coating must be shielded from carbon dioxide exposure during the first 14 d because rapid carbonation reduces pH and solubilises the polymer-cement interphase; water with a Langlier Saturation Index below −0.5 should not be stored unless the cement matrix has been fully carbonated and re-passivated; and the contact water pH must remain above 6.8 to avoid progressive lime leaching that increases porosity and TOC release.
Elevator pits and industrial sumps present a severe environment in which the waterproofing lining is constantly exposed to standing water, intermittent oil contamination, and limiting access for surface preparation. The ability of CELVOLIT 1318-modified mortars to maintain wet adhesion on permanently damp concrete is governed by the polymer-cement ratio and the film coalescence mechanism under high humidity. Formulations for this duty adopt a solid p/c of 0.70–0.90, translating to an emulsion addition of 127–164 parts per 100 parts cement, which yields a continuous polymer network that accommodates the osmotic pressure at the cement-polymer interface during prolonged water immersion. The powder base is a blend of CEM I 42.5 N with fly ash (15 %) and a combination of quartz flour and 0.2–0.5 mm aggregate to improve crack resistance. In the field, the two-component mix is combined with a hand-held paddle mixer operating at 600 rpm and must be placed within a working time of 30 min when ambient temperature reaches 30 °C. After substrate cleaning to remove laitance and oil residues, a thin scratch coat is scrubbed into the saturated surface, immediately followed by embedding an alkali-resistant glass fibre mesh (80 g/m²), and then a top layer applied at 90 min interval to a total dry thickness of 3.0 mm. Wet adhesion is evaluated according to EN 1542 after 7 d water immersion, with a minimum required pull-off strength of 0.8 N/mm²; failure mode must be cohesive in the substrate or the coating. A complementary test per EN 14891 for water impermeability under 0.2 N/mm² for 7 d confirms zero leakage across the lining. The system is not suited for substrates heavily contaminated with mineral oils: a preliminary coating of a two-component epoxy primer is mandatory when oil stains remain after mechanical cleaning. The finished product type remains the standard two-component kit, labelled for waterproofing sumps, cable trenches, elevator pits, and other subsurface utility structures. Exposure to vehicle traffic or mechanical loads is permissible only after a curing period of 7 d at a compressive strength of at least 20 N/mm², and the lining must be protected from freezing for the first 72 h; residual water ponding on the surface during the initial 24 h of curing must be removed to prevent polymer skin at the surface that becomes soft on re-wetting.
| Application Field | Key Standard(s) | Test Method / Requirement | Acceptance Criterion |
|---|---|---|---|
| Interior wet-area behind-tile waterproofing | EN 14891:2017 | Water impermeability under positive 0.2 N/mm² for 24 h (clause 7.2) | No water penetration |
| Interior wet-area behind-tile waterproofing | EN 14891:2017 | Tensile adhesion after water immersion (clause 7.5) | ≥0.5 N/mm² |
| Exterior balcony crack-bridging membrane | EN 14891:2017 | Crack-bridging ability at −5 °C (clause 7.6) | ≥0.75 mm |
| Exterior balcony crack-bridging membrane | EN 13687-4 | Adhesion after freeze-thaw cycling | ≥0.5 N/mm² |
| Swimming pool shell waterproofing | EN 1504-2:2004 (principles 1.3, 6.1) | Water absorption (capillary) – EN 1062-3 | <5 % |
| Swimming pool shell waterproofing | EN 14944-1:2006 (where potable water contact) | Migration of TOC – Annex B | <2.5 mg/L |
| Negative-side basement wall waterproofing | EN 1504-2:2004 (principle 1.3) | Water penetration under 0.5 N/mm² for 72 h (EN 12390-8 modified) | Penetration depth <20 mm |
| Negative-side basement wall waterproofing | EN 1542 | Adhesion on concrete (saturated) after water immersion | ≥0.8 N/mm² |
| Potable water storage tank coating | EN 14944-1:2006 | Migration test for organic substances – Annex B | TOC <2.5 mg/L |
| Potable water storage tank coating | EN 1542 | Adhesion on saturated concrete after 7 d water immersion | ≥0.8 N/mm² |
| Elevator pit sump waterproofing | EN 14891:2017 | Water impermeability under positive 0.2 N/mm² for 7 d | No leakage |
| Elevator pit sump waterproofing | EN 1542 | Wet adhesion after 7 d water immersion | ≥0.8 N/mm² |
| Solid Polymer-Cement Ratio (p/c) | Tensile Adhesion Strength (EN 1542, N/mm²) | Water Absorption (EN 1062-3, %) | Crack Bridging at −5 °C (EN 14891, mm) | Water Penetration under 0.5 MPa (EN 12390-8, mm) |
|---|---|---|---|---|
| 0.40 | 2.1–2.5 | 6.0–8.0 | 0.2–0.4 | 25–35 |
| 0.55 | 1.8–2.2 | 4.5–6.0 | 0.5–0.7 | 15–22 |
| 0.75 | 1.4–1.8 | 3.0–4.5 | 0.8–1.1 | 8–14 |
| 1.00 | 1.0–1.4 | 2.5–3.5 | 1.2–1.6 | 5–10 |
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The integration of vinyl acetate-ethylene (VAE) copolymer emulsions into polymer-modified cementitious waterproofing slurries has become standard practice where flexibility, adhesion, and crack-bridging capability exceed the performance ceiling of unmodified mortars. CELVOLIT 1318 is a carboxylated VAE dispersion engineered specifically for two-component polymer cement waterproofing coatings, supplied as an anionic-stabilized aqueous emulsion with a nominal solids content of 55 ± 1 % and a Brookfield viscosity at 20 °C (spindle 4, 20 rpm) in the range of 1500–4000 mPa·s. The dispersed phase exhibits a glass transition temperature (Tg, midpoint by DSC per ISO 11357-2) of approximately −3 °C, imparting low-temperature film-forming characteristics without external coalescing solvents. Minimum film formation temperature (MFFT, ISO 2115) is < 1 °C, a critical parameter that permits on-site mixing and application under cold-weather conditions where styrene-acrylic alternatives with MFFT above 10 °C may require temporary heating or solvent addition, practices incompatible with enclosed spaces and current VOC directives.
The product is delivered at a pH of 4.0–5.5, stabilized with a non-alkylphenol ethoxylate (non-APE) surfactant system compliant with EU Regulation 1907/2006 (REACH) Annex XVII restrictions. Mechanical stability under high-shear mixing—typical of paddle-type mortar mixers operating at 300–600 rpm—is rated for continuous agitation durations up to 20 minutes without irreversible coagulum formation. However, prolonged pumping through progressive cavity pumps with stator-rotor clearances below 0.5 mm has been observed on certain production lines to generate localized heating exceeding 45 °C, at which point the emulsion can undergo partial thermal destabilization; inline temperature monitoring and a recirculation loop with a heat exchanger are recommended when transfer distances exceed 50 m.
The differentiation resides in the chemical anchoring mechanism within the hydrating cement pore solution. Carboxyl groups present on the CELVOLIT 1318 polymer backbone undergo ionic complexation with divalent calcium ions (Ca²⁺) liberated during alite (C₃S) and belite (C₂S) hydration. This complexation forms a network of ionic crosslinks between the polymer particles and the inorganic cement gel, yielding a co-continuous microstructure rather than a simple interpenetrating network. In contrast, non-carboxylated styrene-butyl acrylate copolymer emulsions rely predominantly on physical encapsulation of cement grains and film coalescence upon drying; when immersed in water, the polymer-cement interface can undergo hydrolytic delamination, leading to a drop in wet adhesion strength below 0.5 MPa as measured by pull-off tests per EN 14891 A.6.2. CELVOLIT 1318-modified compositions, formulated with a polymer-cement ratio (p/c) of 0.20–0.35, retain wet adhesion values exceeding 1.0 MPa on standard concrete substrates after 28 days of water immersion at 23 ± 2 °C, and often exhibit substrate-cohesive failure rather than adhesive rupture, indicating the waterproofing membrane bond outlasts the concrete tensile strength.
| Property | Test Standard | CELVOLIT 1318 at p/c 0.30 | Styrene-Acrylic Emulsion (p/c 0.30) |
|---|---|---|---|
| Water impermeability (positive-side pressure, 0.75 MPa/7h) | EN 14891 A.7 | No penetration | No penetration |
| Crack bridging ability at 23 °C (mm) | EN 14891 A.8.1 | 0.92 ± 0.08 | 0.48 ± 0.12 |
| Crack bridging ability at −5 °C (mm) | EN 14891 A.8.2 | 0.63 ± 0.11 | 0.10 ± 0.05 |
| Adhesion after water contact (MPa) | EN 14891 A.6.2 | 1.15 (cohesive failure) | 0.62 (adhesive failure) |
| Chloride ion penetration depth (mm, ASTM C1543) | ASTM C1202 modified | 3.2 | 7.9 |
Formulators must note that the carboxylation density of CELVOLIT 1318 also accelerates cement hydration kinetics. Isothermal calorimetry data at 23 °C reveal a shortening of the induction period by approximately 45 minutes relative to a non-carboxylated VAE and a corresponding increase in the main hydration peak height by 12–18 %. This effect demands adjustment of the retarder dosage in the dry-mix component, particularly where the liquid polymer is batched on-site rather than as a pre-calibrated factory blend. A typical retarding agent, such as sodium gluconate at 0.05–0.15 wt% of binder, re-establishes open time to 60–90 minutes without compromising 28-day compressive strength.
Waterproofing coatings applied over green concrete or substrates with high residual moisture content present a persistent field failure mode: incomplete film coalescence of the polymer phase. CELVOLIT 1318, with an MFFT below 1 °C and a relatively high ethylene content (estimated in the range of 15–20 % by monomer feed ratio), forms a coherent film even when capillary pore water in the substrate maintains a relative humidity above 85 % at the interface. The film formation mechanism transitions from particle deformation to continuous film through water evaporation and capillary pressure-driven compaction; the low Tg ensures sufficient particle mobility even at 10 °C substrate temperature, a common condition in underground parking structures during autumn. Published failure analysis reports on construction projects where styrene-acrylic-based waterproofing slurries were applied at substrate temperatures below 12 °C document micro-crazing and pinholing attributed to arrested coalescence, detectable by water-spray dye penetrant testing within 48 hours of application. In contrast, field data from polymer-modified slurries based on CELVOLIT 1318 applied at 8 °C and 80 % RH show continuous film formation and absence of interconnected porosity when examined by cross-sectional SEM at 500× magnification.
This performance domain extends to the moisture vapor transmission rate (MVTR) of the cured membrane. Per EN ISO 7783-2, a CELVOLIT 1318-modified cementitious coating (dry film thickness 2.0 mm) exhibits an MVTR in the range of 15–25 g/(m²·d), classifying it as breathable yet liquid-water-tight. Such transmission rates are essential for “negative-side” waterproofing applications on earth-retaining structures, where hydrostatic pressure can force water between the concrete substrate and a fully impermeable, vapor-closed membrane, causing blistering. The MVTR is tunable by adjusting the p/c ratio: at p/c 0.20, MVTR drops to approximately 10 g/(m²·d); at p/c 0.40, it rises to 30–35 g/(m²·d), but wet adhesion after 14 days of water immersion begins to decline if the ratio exceeds 0.38, likely due to dilution of the cement gel matrix continuity.
| Key Specification | CELVOLIT 1318 Value | Test Method |
|---|---|---|
| Solids content | 55 ± 1 % | ISO 3251 (2 h at 105 °C) |
| Viscosity (Brookfield RVT, 20 rpm, 23 °C) | 1500–4000 mPa·s | ISO 2555 |
| pH | 4.0–5.5 | ISO 976 |
| Glass transition temperature (Tg) | −3 ± 1 °C | ISO 11357-2 (DSC, 10 K/min) |
| Minimum film formation temperature | < 1 °C | ISO 2115 |
| Particle size (D50) | 0.8–1.2 µm | Laser diffraction (ISO 13320) |
| Stabilizer type | Anionic, non-APE surfactant | – |
| Storage stability (sealed container, 5–35 °C) | 12 months from date of manufacture | Visual, no settling > 1 mm |
Specifications listed are typical lot average values and do not constitute guaranteed limits. Production batches are subject to internal quality control ranges that align with the above test methods; certificates of analysis accompany each shipment referencing these ISO procedures.
The emulsion contributes significantly to the rheological profile of the mixed slurry. At a standard mix proportion of 1 part liquid polymer : 4 parts powder (by weight), the resulting slurry exhibits shear-thinning behavior with a dynamic viscosity at 10 s⁻¹ of approximately 3000–5000 mPa·s and at 100 s⁻¹ of 800–1500 mPa·s (measured by a rotational rheometer with parallel plate geometry, gap 1 mm, 23 °C). The pronounced pseudoplasticity ensures that the material flows readily during trowel or roller application yet resists sag when placed on vertical surfaces at wet film thicknesses up to 2.5 mm. Sag resistance tested per a modified ASTM D4400 procedure (notched sag gauge, 2 mm clearance) at 20 °C and 65 % RH yielded zero sag at wet thicknesses up to 2.0 mm. For spray application via airless piston pumps (e.g., Graco GH 130 or equivalent with a 40:1 ratio pump), the shear-viscosity reduction under tip shear rates of 1000–5000 s⁻¹ enables atomization with tip sizes as small as 0.021 in (0.53 mm), though a 0.025–0.027 in orifice is recommended for sustained production throughput above 3 L/min.
Experienced applicators report that the open time of CELVOLIT 1318 slurries, defined as the interval during which a fresh bead of material can be blended into the preceding pass without a visible cold joint, ranges from 25 to 40 minutes at 23 °C and 50 % RH. This window is shorter than that of some purely acrylic liquid modifiers, which can remain workable for over 60 minutes but exhibit greater sensitivity to plastic cracking due to slower setting. The shorter open time is a direct consequence of the accelerated cement hydration noted above, and it should be factored into crew size planning; a 3-person gang (one mixer, one applicator, one finisher) typically manages a continuous application rate of 15–20 m²/h for a two-coat system with embedded reinforcement mesh.
When outdoor application is required on open terraces or balconies, the slurry’s susceptibility to early rain wash-out is a critical field concern. The combination of rapid cement stiffening due to carboxylate-induced acceleration and polymer film formation at the surface reduces wash-out risk compared to EVA powder-modified mortars that rely solely on redispersible powders. Simulated rainfall testing (water spray at 50 mm/h intensity applied 2 hours after troweling at 1.5 mm thickness) on a CELVOLIT 1318 mortar at p/c 0.30 resulted in less than 3 % mass loss, versus 18–25 % mass loss for a comparable formulation using a commercial VAc/VeoVa redispersible powder at a polymer content of 10 wt% of the dry mix. This resilience is directly transferable to job sites in regions with unpredictable weather patterns and eliminates the need for temporary rain-shielding measures for short-duration storm events.
Several processing pitfalls have been catalogued from technical service interventions on active manufacturing and application sites. One recurring issue involves the over-dilution of CELVOLIT 1318 with water at the job site to extend pot life or improve trowel slip. Dilution to a polymer solids content below 45 % in the liquid component (i.e., adding more than 20 parts water per 100 parts emulsion) disrupts the ionic balance and can cause a sharp drop in wet adhesion down to 0.3 MPa or lower because the polymer-cement ratio in the cured film shifts out of the optimal interlocking range. Quality control protocols should strictly prohibit uncontrolled water addition; if flowability must be increased, a dispersion-compatible superplasticizer (polycarboxylate ether, PCE, at 0.1–0.3 % on cement weight) should be incorporated into the powder component instead. A second failure mode arises when the emulsion is exposed to repeated freeze-thaw cycles during transport in unheated trucks. Although the emulsion is protected against freezing by formulation, extended exposure to temperatures below −5 °C for more than 48 hours can induce irreversible viscosity increase and microscopic gel particles visible on a Hegman gauge at 50 µm. Containers should be stored indoors at 5–35 °C; thawing of inadvertently frozen product must be performed slowly at 20–25 °C over 24–48 hours, accompanied by low-shear agitation at 100 rpm. High-shear mixing of thawed material without adequate rest can destroy the remaining shear-stable fraction, resulting in macroscopic phase separation.