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Anhui Liwei Chemical Co., Limited.

Flexible RDP for C2TES1 Tile Adhesives

    • Product Name: Flexible RDP for C2TES1 Tile Adhesives
    • 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 356193
    Chemical Composition Vinyl acetate-ethylene (VAE) copolymer
    Physical Form Free-flowing white to off-white powder
    Redispersibility Fully redispersible in water to form a stable emulsion
    Minimum Film Formation Temperature Approximately 5 °C
    Particle Size d50 50–80 µm, 80% passing 200 mesh
    Bulk Density 450–550 g/L
    Ash Content 10–15%
    Ph 10 Aqueous Dispersion 7.0–8.5
    Adhesion Strength Contribution Supports achieving C2 classification with tensile adhesion strength ≥ 1.0 N/mm²
    Deformability Contribution Supports S1 classification with lateral deformation ≥ 2.5 mm
    Slip Resistance Contribution Improves sag resistance for vertical tile application (T class)
    Open Time Contribution Supports extended open time of at least 30 minutes (E class)

    As an accredited Flexible RDP for C2TES1 Tile Adhesives factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Flexible RDP for C2TES1 tile adhesives, supplied in 25 kg moisture-protective multi-layer paper bags for easy handling and storage.
    Container Loading (20′ FCL) 20′ FCL shipment of Flexible RDP for C2TES1 tile adhesives, packed in sealed bags on pallets, ensuring safe, efficient transport.
    Shipping Flexible RDP for C2TES1 tile adhesives is shipped as a free-flowing powder in 25 kg multi-layer paper bags, palletized and shrink-wrapped for transit. Protect from moisture and direct sunlight; store in a cool, dry area below 30°C. Non-hazardous, safe for standard container transport. Avoid exposure to rain.
    Storage Store Flexible RDP in a cool, dry, well-ventilated area, away from direct sunlight, heat, and moisture. Keep sealed in original bags on pallets, avoiding floor contact. Use within 12 months; protect from humidity and water ingress. Follow safe handling and local regulations.
    Shelf Life Shelf life: 12 months from manufacture when stored unopened in original packaging, kept cool, dry, and protected from moisture.
    Application of Flexible RDP for C2TES1 Tile Adhesives

    Differential movement generated by hydronic underfloor heating is the first application context in which flexible RDP influences C2TES1 performance. The bonded assembly consists of a calcium sulphate or cementitious screed, a direct-bonding or uncoupling layer, the C2TES1 adhesive, and large-format porcelain panels with edge lengths frequently beyond 900 mm and thicknesses between 6 mm and 9 mm. The adhesive joint must accommodate linear thermal expansion differences between the screed and the vitrified tile body; when screed surface temperature cycles from 20°C to 45°C, the tile-adhesive interface is placed in shear at the tile edge. A flexible vinyl acetate-ethylene redispersible polymer powder with a film-forming content in the range of 2.5–4.0 wt% on total dry mortar modifies the cured matrix by depositing a low-modulus polymer film through the cementitious pore structure. In formulation terms, a C2TES1 dry mix for this application is commonly built from 32–38 wt% CEM I 52.5R, 55–62 wt% graded silica sand with a 0.1–0.5 mm d90, 2.5–4.0 wt% flexible RDP, 0.4–0.6 wt% cellulose ether, and 0.1–0.3 wt% polycarboxylate ether powder. The wet mortar is mixed with 22–26 wt% water based on dry material, left to slake for 3–5 minutes, remixed, and applied with a notched trowel selected to achieve not less than 80% contact behind large-format tiles. Back-buttering with a thin contact layer is mandatory for tiles with edge length above 600 mm to avoid void formation. The terminal product is a heated floor covering with grout joint widths of 1.5–3 mm that maintains tensile adhesion above 1.0 MPa after heat ageing when tested according to EN 1348. Published data for this specific configuration is limited to laboratory and field pull-off tests; batch-to-batch variance in polymer glass transition temperature can shift the transverse deformation result under EN 12002 by several tenths of a millimetre.

    Does Pool Waterline Exposure Demand a Higher RDP Dosage Than Standard Wet Areas?

    The waterline of a swimming pool is not a standard wet area because constant immersion is interrupted by drying and chlorinated water movement. C2 classification under ISO 13007-2 requires tensile adhesion of not less than 1.0 MPa after water immersion when evaluated by EN 1348, and the E criterion demands not less than 0.5 MPa after an extended open time of at least 30 minutes. For waterline mosaic and ceramic tile installations, flexible RDP dosage is typically maintained at 3.0–4.5 wt% of dry mortar because sustained water saturation softens some polymer films and the tile bed must retain shear capacity at the waterline curvature. The mortar formulation uses a lower water-to-powder ratio of 21–24 wt% to reduce capillary porosity, and the blend includes 0.5–0.8 wt% cellulose ether to prevent rapid water loss during wet-on-wet application over waterproofing membranes. T classification under EN 1308 requires vertical slip not exceeding 0.5 mm, which is relevant when fixing glass mosaics with paper face mounting. The application sequence requires a solvent-free epoxy or cementitious waterproofing membrane, a notched trowel with tooth depth of 3–4 mm for mosaics or 8–10 mm for larger porcelain pieces, and pressing the tile into the adhesive bed with a flat beating block to reduce trapped air. Hypochlorite-based pool sanitizers can oxidize exposed polymer film at the grout joint over long service periods; published data for this specific configuration is limited, and the use of a hydrophobic copolymer grade is preferred over high-vinyl acetate homopolymer-type powders. The finished product is a submerged-ready tile wall with movement joints at coving intersections and at the waterline level, with grout selected for constant immersion and with no flexible RDP film exposed to permanent ultraviolet degradation because the adhesive is fully shielded by tile and grout.

    Façade Cladding Over Cement-Bonded Board and Gypsum Fibre Substrates

    Cement-bonded board and gypsum fibre substrates impose a combination of high suction, low surface roughness, and structural movement that a C2TES1 adhesive must tolerate without losing bond. For ventilated façades, the adhesive joint is exposed to wind-induced vibration and to rapid surface drying before the tile is placed. Flexible RDP in the range of 3.0–4.5 wt% is used because the S1 deformability requirement under EN 12002 of at least 2.5 mm transverse deformation reduces the risk that substrate deflection cracks telegraph into the tile. The dry mix is adjusted with 0.3–0.5 wt% cellulose ether for water retention and 0.05–0.2 wt% starch ether to control slip on vertical planes. Mixing at the jobsite uses a slow-speed paddle mixer at 300–500 rpm rather than a high-shear colloidal mixer, because high shear can destabilize the redispersed polymer phase and reduce wet density. Application over gypsum fibre board requires priming with an acrylic or cementitious primer to even out suction and to prevent the formation of calcium sulphate at the interface; unprimed gypsum fibre can extract moisture fast enough to leave a polymer-cement film that is cohesive but not adhesive to the board. The adhesive is trowelled with a 6×6 mm to 10×10 mm square-notch comb, and the back of each tile is buttered if panel size exceeds 600×600 mm. The terminal product is a façade tile field fixed in a continuous bed with movement joints at floor-to-floor levels and vertical joints at building movement lines, with tensile adhesion after heat ageing and freeze–thaw conditioned in accordance with EN 1348 and EN 12004:2017 remaining above 1.0 MPa for the C2 classification.

    When Old Vitrified Tile Is Retained as Substrate for a New C2TES1 Bonding Layer

    Retention of existing vitrified tile eliminates demolition dust and waste but introduces a non-absorbent, often polished substrate that can retain cleaning agents and siliconates. The C2TES1 adhesive is therefore formulated at the higher end of flexible RDP content, typically 3.5–4.5 wt%, to compensate for the absence of mechanical key and to provide some accommodation of stress from the differential movement between the old tile and the new covering. Preparation starts with mechanical abrasion of the existing surface to remove glaze gloss, followed by washing with a low-residue alkaline detergent and rinsing until no film remains. A primer based on an acrylic dispersion or two-component cementitious slurry is applied and allowed to cure; the adhesive is then spread with a notch depth of 8–12 mm depending on floor flatness, but the final bed thickness after pressing should not exceed 10 mm unless the formulation has been screened for shrinkage. The E classification is operationally important because the non-absorbent substrate delays water removal and can extend the period before the adhesive begins to set; open time is evaluated by EN 1348 after a 30-minute exposure. Slip resistance under EN 1308 is equally required when wall tile is installed over existing tile in renovation bathrooms. The terminal product is a new tile or stone layer bonded to an existing tile base with the original tile joints filled or levelled before adhesive application; the C2TES1 adhesive must remain below 1.0 MPa internal stress at the old substrate interface, which is why polymer film coalescence must be allowed to occur before water immersion or thermal loading. Published data for this specific configuration is limited for relative humidity below 40%; in such conditions, the drying rate exceeds film coalescence and adhesion to the old glaze can drop noticeably.

    In a retail concourse with rubber-wheeled trolley traffic and concentrated point loads at floor drains, the C2TES1 adhesive is required to resist cyclic compressive and shear loads without delaminating. The adhesive layer is applied at a nominal thickness of 3–6 mm, but actual thickness varies due to floor flatness and the need to achieve full contact under large-format porcelain stoneware. Flexible RDP content tends towards the upper end of 3.0–4.5 wt% because S1 deformability and vibration absorption are needed under rolling loads. The dry mix is based on 30–35 wt% CEM I or CEM II/A-LL 42.5R, 55–65 wt% graded quartz, 3.0–4.5 wt% flexible VAE RDP, 0.3–0.5 wt% cellulose ether, 0.2–0.4 wt% calcium formate accelerator where night work requires early setting, and 0.05–0.2 wt% starch ether for anti-sag. Calcium formate beyond 0.5 wt% is not recommended where S1 deformability is required, as rapid early hydration can limit polymer film coalescence. T classification tested per EN 1308 is not a generic slump value but a quantified vertical slip limit of ≤0.5 mm after trowelling and tile application. The terminal finished floor includes porcelain stoneware slabs with rounded profiled edges, expansion joints at bay sizes not exceeding 25 m², and urethane or epoxy grout in high-load aisles. A forced-action mixer at 500 rpm for 300–600 kg batches reduces air entrapment; extended mixing beyond 3 minutes at high shear may destabilize the redispersed polymer and lower wet density. Testing for tensile adhesion after water immersion and freeze–thaw is carried out according to EN 1348, and the adhesive joint is expected to remain above 1.0 MPa to satisfy EN 12004:2017 C2.

    ISO 13007-2 C2TES1 verification matrix relevant to flexible RDP formulation
    CharacteristicStandard / methodConditionMinimum requirement
    Tensile adhesion after standard cureEN 1348Defined curing under standard conditions≥1.0 MPa
    Adhesion after water immersionEN 1348Water immersion after standard cure≥1.0 MPa
    Adhesion after heat ageingEN 1348Elevated-temperature storage after defined cure≥1.0 MPa
    Adhesion after freeze–thawEN 1348Freeze–thaw cycles after specified cure≥1.0 MPa
    Extended open time tensile adhesionEN 1348Not less than 30 min after trowelling≥0.5 MPa
    Transverse deformationEN 12002After defined curing≥2.5 mm and <5.0 mm
    Slip resistanceEN 1308Vertical loading after combing≤0.5 mm

    Balcony Installations Fail First at the Perimeter Joint, Not the Tile Centre

    A balcony assembly expands and contracts across a larger thermal envelope than interior tile, and the perimeter joint concentrates the resulting strain. The C2TES1 adhesive must maintain shear adhesion over a waterproofing membrane while the entire sandwich experiences daily surface temperature swings from −10°C to 50°C in temperate climates and wider ranges in alpine or gulf environments. Flexible RDP content is typically 3.0–4.5 wt%, and the transverse deformation characteristic under EN 12002 is maintained at ≥2.5 mm but not high enough to enter S2; an S2-flexible adhesive may not be required and can show lower compressive rigidity under point loading. The waterproofing membrane below the adhesive must be compatible with cementitious mortar; solvent-borne liquid membranes are generally avoided unless fully cured and primed. Application uses a 10 mm or 12 mm rounded notch trowel, with full coverage achieved by double-buttering because hollow spots under balcony tile become freeze–thaw fracture origins. The terminal product is a balconied tile surface with perimeter movement joints of 5–10 mm width, filled with elastic polyurethane sealant, and intermediate movement joints at intervals not exceeding 3–4 m. The adhesive must pass freeze–thaw conditioning of EN 1348 with tensile adhesion not less than 1.0 MPa after cycling, while slip resistance under EN 1308 remains below 0.5 mm on sloped balcony surfaces during installation. Published data for this specific configuration is limited when balcony slabs carry heavy planters or glass balustrade point loads at the edge; point loads can exceed 2 kN and require structural isolation rather than relying on the adhesive’s S1 deformation.

    To Extend Open Time Beyond 30 Minutes in High-Rise Façade Work Without Losing Slip Resistance

    Above 30°C ambient temperature, a C2TES1 mortar that passes standard open-time testing under laboratory conditions can still skin on a high-rise balcony or façade if wind speed exceeds 2 m/s and relative humidity drops below 35%. The E classification demands tensile adhesion not less than 0.5 MPa after an open time of at least 30 minutes when tested under EN 1348, but field open time can be shorter due to radiative heat from glass and metal framing. To extend open time without losing slip resistance, the formulation is balanced with 0.5–0.8 wt% cellulose ether, 3.0–4.0 wt% flexible RDP, and a low-dose retarder such as tartaric acid or sodium gluconate at 0.02–0.05 wt% where cement hydration rate must be adjusted. Increasing cellulose ether alone improves water retention but can reduce slip resistance and lower early adhesion; increasing RDP alone may increase open time slightly through film-forming water barriers, but it also reduces wet density and can increase cost and tack. The mixing procedure in hot weather uses chilled water below 15°C, a two-stage mix at 300 rpm for 60 seconds, slaking for 5 minutes, and a final mix at 300 rpm for 60 seconds to stabilize air content. The adhesive is applied in small sections and the tiler must test surface skinning frequently; when a fingertip no longer transfers adhesive, the material is removed rather than re-trowelled with additional water. The terminal finished product is a high-rise tile façade with full contact under each tile, open-time compliance documented by site pull-off tests, and no evidence of hollow panels under thermal imaging. Published data for this specific configuration is limited above 30°C ambient temperature; the open-time requirement can fall below 20 minutes unless windbreaks or shade are used.

    Resin-backed natural stone agglomerates and large-format glass mosaics reverse the usual moisture problem because the adhesive must transfer moisture through a dense or impervious tile without staining the surface. A C2TES1 adhesive with flexible RDP at 3.0–4.5 wt% is used in hotel lobbies and reception areas where slabs may be 1200×1200 mm or larger and are bonded over metal or wooden transition strips. The formulation is deliberately lean in free water, mixed at 20–23 wt% water, and may include 0.2–0.4 wt% of a defoamer to prevent pinholes in large-format glass installations. The adhesive is spread with a 8 mm or 10 mm notch trowel, and the tile back is buttered with a thin layer to fill ribs and cavities in resin-backed stone. Terminal products include polished stone floors with narrow grout joints of 2–3 mm and glass mosaic feature walls with translucent areas that require full adhesive coverage to avoid shadow lines. Mortar bed thickness is maintained between 3 mm and 6 mm; thicknesses above 10 mm require consultation with the powder supplier because polymer-enriched thick sections can retain moisture and delay early strength development. The adhesive is tested under EN 1348 for adhesion to both the substrate and the resin or glass back, and a site-specific spalling check is recommended because moisture-sensitive stone may etch or discolour if the polymer film remains wet for prolonged periods. Published data for this specific configuration is limited for glass mosaics with ceramic frit backings; adhesion values can vary from 0.8 MPa to above 1.0 MPa depending on frit composition and surface energy.

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    Certification & Compliance
    More Introduction

    Flexible RDP for C2TES1 Tile Adhesives is a redispersible polymer powder based on a carboxylated vinyl acetate–ethylene/vinyl ester copolymer, assigned model designation RDP-FC2TES1-15. The grade is specified with a bulk density of 420–560 kg/m³, residual moisture below 1.2 wt%, ash content of 11–13 wt% after 2 h at 1000 °C, and a minimum film-forming temperature of 0–2 °C. The product is intended as the primary polymer modifier in cementitious dry-mix formulations classified under EN 12004-1:2017 as C2TES1. To meet that designation, the adhesive must demonstrate initial tensile adhesion of at least 1.0 N/mm² after 28 days of standard curing and retain at least 1.0 N/mm² after water immersion, heat ageing, and freeze–thaw cycling when tested according to EN 1348. Additional classifications require a vertical slip of no more than 0.5 mm according to EN 1308, an open time adhesion of at least 0.5 N/mm² after 30 min according to EN 1346, and transverse deformation between 2.5 mm and 5.0 mm according to EN 12002.

    What Must a Flexible Redispersible Powder Deliver in a C2TES1 Matrix?

    In a C2TES1 dry-mix, the redispersible polymer is required to form a continuous film that bridges microcracks in the cementitious matrix and absorbs shear strain at the tile–substrate interface. The glass transition temperature of −12 °C to −16 °C allows film formation at ambient application temperatures and maintains deformation above the S1 threshold. During cement hydration, polymer particles adsorb onto cement grains and coalesce into a network that interpenetrates with calcium silicate hydrate phases. The film reduces the modulus of the cured adhesive, lowering the stress transferred to the tile bond line and producing a transverse deformation between 2.5 mm and 5.0 mm under EN 12002.

    The carboxyl groups on the polymer backbone interact with calcium ions released during C3S and C2S hydration. That interaction retards the formation of a brittle interfacial film and improves adhesion to hydrated cement surfaces. The ethylene segments lower the cohesive energy density of the polymer film, producing an elongation at break of approximately 300–500% and a tensile strength of 3.5–5.0 MPa when tested on free films at 0.5 mm dry thickness. These film properties are directly linked to the S1 deformability result because the adhesive layer must tolerate 2.5–5.0 mm transverse deflection without failing in tension.

    Redispersion at 19–21 °C in standard mixing water yields a pseudoplastic dispersion with a Brookfield viscosity of 2,500–3,500 mPa·s at 20 rpm and 50% solids. The polymer’s carboxylation increases wetting of silica sand and cement surfaces, which is necessary for open time retention. In comparison with unmodified mortars, the addition of 3.5 wt% of the product raises wet tensile adhesion and prevents the open time adhesion from falling below 0.5 N/mm² after 30 min in laboratory tests conducted at 23 °C and 50% relative humidity.

    Water immersion resistance is governed by the polymer film’s low water uptake. Water absorption of a cured film, cast at 0.5 mm dry thickness and dried for 14 days at 23 °C, is typically below 10 wt% after 24 h immersion in deionised water. This property contributes to the retention of at least 1.0 N/mm² tensile adhesion after the EN 1348 water immersion protocol.

    Where conventional VAE powders with a glass transition temperature above −5 °C are used in C2 formulations, the extended open time requirement and the S1 deformability requirement frequently conflict. Such powders produce a hard film at tile-adhesive surfaces after 15–20 min, reducing wetting of the tile and causing open time adhesion to drop below 0.5 N/mm² at 30 min. Flexible RDP for C2TES1 Tile Adhesives differs by using a bimodal particle size distribution with a D50 of approximately 70–90 µm and a D90 below 180 µm. The coarse fraction delays full film coalescence, preserving tack during the open time window, while the fine fraction contributes to early cement wetting and rheology control.

    Compared with styrene–acrylate RDP grades, the VAE/VeoVa backbone provides lower water absorption and improved re-dispersibility in high-pH cement pastes. Styrene–acrylate grades may exhibit superior heat-ageing retention in some formulations, but they can require higher addition levels to achieve the same S1 deformation. Published data for this specific configuration is limited; plant trials are therefore used to confirm the optimum ratio when the cement source or aggregate surface area changes.

    Dry-Blend Stability and Production-Scale Mixing Boundaries

    Production-scale blending of the powder requires control of moisture and temperature. In a single-shaft ploughshare mixer operating at 45 rpm, the recommended addition sequence is coarse aggregate, fine sand, limestone filler, cement, cellulose ether, and finally the polymer powder. The addition of the polymer after cellulose ether avoids electrostatic coating of the cellulose ether particles by fine polymer particles, which can delay hydration-controlled viscosity development. A total final mixing time of 180 s is normally sufficient for a 1,000 kg batch, provided the mixer jacket temperature remains below 45 °C.

    On production lines using ribbon mixers, batch-to-batch viscosity drift has been observed when the powder is fed into a vessel receiving warm recycled filler or when the fillers have free moisture above 0.4 wt%. The powder may then partially redisperse on contact with damp aggregate surfaces and form 2–5 mm lumps that do not break down in subsequent dry mixing. Pre-drying of aggregates at 105 °C until free moisture falls below 0.2 wt% is recommended when ambient relative humidity exceeds 70%. The product is packaged in 25 kg multi-wall paper sacks with a polyethylene moisture barrier and should be stored at 5–30 °C in unopened sacks to keep residual moisture below 1.2 wt%.

    On a production-scale twin-shaft continuous mixer with a throughput of 8–12 t/h, the powder feed should be located in the first half of the mixing chamber after the cellulose ether feed. This sequence prevents the polymer powder from being exposed to high-shear choppers for more than 30 s, which can generate sufficient frictional heat to soften the particles above 45 °C and create agglomerates. Batch records from continuous lines show that feed-rate variability above ±5% can produce measurable differences in open time adhesion because the polymer-to-cement ratio shifts locally before homogenisation is complete.

    For field application, a C2TES1 adhesive based on the powder is typically mixed with 240–260 mL of water per 1 kg of dry mortar. The mixing procedure specified in technical data sheets uses a low-speed drill mixer at 400–600 rpm for 120 s, followed by a 5 min slaking period and a final 30 s remix. Wet density at the recommended water addition is 1.45–1.55 kg/L. Pot life at 20 °C and 65% relative humidity is approximately 120 min, measured as the time during which the tensile adhesion after 28 days remains above 1.0 N/mm². Open time under the same conditions is 30 min, with adjustment of the tile possible for up to 20 min after initial placement before the slip requirement is compromised.

    The wet product is applied with a notched trowel; the rib height and notch size must be selected to achieve a contact area of at least 65% for interior dry applications and 90% for exterior or wet areas. The product is designed for tile masses up to 40 kg/m² on vertical surfaces when tested with a 5 mm notched trowel. Above that limit, additional mechanical fixing or a non-slump fast-setting formulation may be required. No additional water should be added after initial slaking; re-tempering reduces polymer film continuity and lowers freeze–thaw resistance.

    When Addition Exceeds the Rheological Threshold, Slip and Deformability Diverge

    In the reference formulation containing 35.0 wt% CEM I 42.5 N, 58.7 wt% quartz sand 0.1–0.6 mm, 0.4 wt% cellulose ether, 0.4 wt% calcium formate, and 3.5 wt% of the flexible powder, the material meets the C2TES1 classification with a margin. Increasing the polymer addition to 4.5 wt% raises transverse deformation further but can reduce the vertical slip threshold because the wet adhesive becomes softer and heavier. In laboratory trials, slip increased from 0.3 mm at 3.5 wt% to 0.6 mm at 4.5 wt% unless starch ether or a high-viscosity cellulose ether was added at 0.05–0.10 wt% of the total dry mix.

    This behaviour represents a rheological threshold: the polymer begins to act as a viscosity modifier and a plasticiser simultaneously. The open time is extended, but the early adhesion before the film has fully coalesced may fall below 1.0 N/mm² if the dosage is pushed above 5.0 wt%. The S1 classification is then met, but the initial tensile adhesion and water immersion adhesion may become inconsistent. The present product is therefore specified at 3.0–4.0 wt% for standard C2TES1 formulations and up to 4.5 wt% only when the formulation includes a compensating rheology package.

    Indicative performance of a C2TES1 dry-mix formulated with 3.5 wt% RDP-FC2TES1-15 versus a conventional VAE grade
    PropertyTest methodFlexible RDPConventional VAE
    Initial tensile adhesionEN 13481.4 N/mm²1.1 N/mm²
    Tensile adhesion after water immersionEN 13481.2 N/mm²0.9 N/mm²
    Tensile adhesion after heat ageingEN 13481.3 N/mm²1.0 N/mm²
    Tensile adhesion after freeze–thaw cyclingEN 13481.1 N/mm²0.8 N/mm²
    Open time adhesion after 30 minEN 13460.8 N/mm²0.5 N/mm²
    Vertical slipEN 13080.3 mm0.6 mm
    Transverse deformationEN 120023.2 mm1.9 mm

    The product should not be combined with solvent-based additives, liquid plasticisers, or film-forming aids added directly to the dry mix, because these components can prevent uniform redispersion of the powder particles. Avoid amine-based additives and strong oxidising agents; the vinyl acetate–ethylene backbone is sensitive to oxidative degradation at temperatures above 70 °C during prolonged storage of the dry mix. Do not use water containing more than 500 ppm chloride or 200 ppm sulfate for mixing; high salt levels can depress cement hydration and alter polymer film coalescence.

    The product is supplied as a non-hazardous powder under Regulation (EC) No 1907/2006 (REACH). The powder does not contain substances of very high concern above 0.1 wt%. For occupational handling, the inhalable dust fraction should be controlled to below 10 mg/m³ as the 8-hour time-weighted average for nuisance dust; use local exhaust ventilation when emptying sacks into silos.

    Compliance checklist for a C2TES1 formulation using RDP-FC2TES1-15 at 3.5 wt%
    RequirementStandardRequired valueLaboratory result
    Initial tensile adhesionEN 13481.0 N/mm²1.4 N/mm²
    Tensile adhesion after water immersionEN 13481.0 N/mm²1.2 N/mm²
    Tensile adhesion after heat ageingEN 13481.0 N/mm²1.3 N/mm²
    Tensile adhesion after freeze–thaw cyclingEN 13481.0 N/mm²1.1 N/mm²
    Vertical slip resistanceEN 13080.5 mm0.3 mm
    Extended open time adhesionEN 13460.5 N/mm² after 30 min0.8 N/mm²
    Transverse deformationEN 120022.5–5.0 mm3.2 mm