| HS Code | 905872 |
| Product Name | ELOTEX MP2100 |
| Product Type | Redispersible Polymer Powder |
| Chemical Type | Vinyl Acetate/Ethylene (VAE) Copolymer |
| Appearance | White, free-flowing powder |
| Bulk Density | 400-600 g/L |
| Particle Size | Approximately 100 µm average; ≤2% residue on 400 µm sieve |
| Ph 10 Aqueous Dispersion | 6.0-8.0 |
| Residual Moisture | ≤1.0% |
| Ash Content | 10-15% |
| Protective Colloid | Polyvinyl Alcohol |
| Anti Blocking Agent | Inorganic Mineral Additive |
| Minimum Film Forming Temperature | Approximately 0°C |
As an accredited ELOTEX MP2100 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | ELOTEX MP2100 is supplied in 20 kg multi-layer paper bags, palletized for safe storage and convenient handling. |
| Container Loading (20′ FCL) | 20-foot FCL shipment of ELOTEX MP2100, packed in 25kg bags on pallets, secured for safe transport. |
| Shipping | ELOTEX MP2100 is a free-flowing polymer powder supplied in moisture-protective bags, typically 25 kg, on shrink-wrapped pallets. It is non-hazardous under standard transport regulations. Protect from humidity, rain, and mechanical damage. Keep pallets dry and store indoors. Avoid excessive heat and direct exposure to moisture during transit. |
| Storage | Store ELOTEX MP2100 in a cool, dry area away from direct sunlight and sources of heat. Keep the container tightly sealed to prevent moisture absorption, which can cause caking or loss of performance. Avoid exposure to high humidity and frost. Use within the recommended shelf life, typically 12 months from delivery when stored properly. |
| Shelf Life | Store in original packaging, cool and dry. Shelf life is 12 months from date of manufacture. |
ELOTEX MP2100 is handled as a free-flowing redispersible vinyl acetate-ethylene copolymer powder with residual moisture below 2.0 wt% and bulk density typically in the 450–600 g/L range. In cementitious tile adhesive production targeting classification C1 or C2 under ISO 13007-1:2014, the powder is dry-compounded with ordinary Portland cement 42.5 N or 42.5 R, graded silica sand from 0.1 mm to 0.5 mm, limestone filler, methyl hydroxyethyl cellulose, calcium formate accelerator, and, where slip control is required, a starch ether or sepiolite thickener. The dry blend is mixed in a twin-shaft paddle mixer at 15–25 rpm for 8–12 min, then passed through a lump breaker before bagging; plant relative humidity is maintained below 70% and product temperature is kept below 40 °C to prevent moisture uptake and premature re-dispersion of the powder. ELOTEX MP2100 is typically dosed at 2.0–4.0 wt% of the dry formulation. At 2.0 wt%, the powder improves wetting and adhesion but may not provide sufficient deformability for C2 classification under thermal ageing. At 3.0 wt%, the formulation is usually positioned for C2 tensile adhesion and open time, while 4.0 wt% increases water retention and open time but raises low-shear viscosity and extends drying. The interaction with methyl hydroxyethyl cellulose is process-critical: cellulose ether at 0.3–0.5 wt% builds anti-sag character and water retention, but overdosing above 0.6 wt% competes with the polymer powder for free water and can produce a sticky, heavy trowel feel. Site mixing is carried out by adding the dry blend to a measured water volume in a forced-action paddle mixer at 300–500 rpm for 2 min, slaking for 5 min, and remixing for 30 s. The mixed adhesive is applied with a notched trowel, and tile bedding is checked after pressing with a twisted motion; open time is evaluated against EN 1346, while tensile adhesion is tested by pull-off according to EN 1348 after the conditioning regimes defined in ISO 13007-2. The powder is not recommended at loadings above 4.5 wt% in standard C1 tile adhesives because early compressive strength falls and bag storage above 30 °C can cause powder blocking in humid warehouses.
In calcium sulfate-based self-leveling underlayments produced to EN 13813:2002, flow retention is governed by the competition between high early dissolution of sulfate binder and the water-binding action of the redispersible powder. ELOTEX MP2100 is dry-compounded at 1.5–3.5 wt% with alpha-hemihydrate or anhydrite binder, silica sand from 0.1 mm to 0.3 mm, limestone powder, a low-viscosity polycarboxylate ether superplasticizer, defoamer, and, where set adjustment is required, sodium gluconate or citric acid retarder. The powder is added before the superplasticizer because simultaneous addition can generate high-shear agglomerates that survive twin-shaft mixing and later appear as surface pinholes during trowelling. The mortar is pumped through a continuous rotor/stator mixer with water dosing adjusted to a flow ring diameter of 130–150 mm measured by the EN 12706 ring; the applied layer is spike-rolled to release air. At 3.0 wt%, MP2100 reduces plastic shrinkage cracking and surface dusting, but it cannot correct a formulation deficiency caused by excessive binder fines below 0.063 mm, because such fines consume water and produce early calcium sulfate nucleation. Flow retention is validated by ASTM C1708/C1708M-19 with a 300 mm flow cone or the EN ring; production formulations usually target an initial flow loss of less than 20 mm over 20 min at 23 ± 2 °C. If the dosage exceeds 4.0 wt%, the wet mix thickens and compressive strength can fall below the C25 or C30 requirements in EN 13813 for commercial traffic areas. Published data specific to MP2100 in anhydrite flowing screeds is limited, and formulators generally validate via EN 13813 type testing rather than extrapolating from tile adhesive data.
The base coat mortar in external thermal insulation composite systems (ETICS) is compounded with ELOTEX MP2100 at 2.5–5.0 wt% into a dry mix containing cement 32.5 R, limestone filler, silica sand, cellulose ether, and a hydrophobic additive such as metal stearate. The mortar is mixed on-site in a forced-action mixer and applied to expanded polystyrene boards at 3–5 mm base coat thickness; alkali-resistant glass fibre mesh is embedded while the surface remains wet, and a second pass closes the mesh. The polymer powder provides adhesion to the EPS substrate and controls crack propagation across the mesh junction, but this function is only realised if the wet mortar remains workable for at least 20 min at 15–25 °C; adding a high cellulose ether dose alone thickens the mix without improving mesh embedment. The cured render is evaluated under ETAG 004 or EAD 040083-00-0404 using hard body impact tests at 3 J and 10 J; formulations with MP2100 below 2.5 wt% frequently show brittle mesh imprint marks and debonding at the EPS-render interface after heat-rain cycles. The manufacturing bottleneck is overmixing in the dry plant: pre-gelatinized starch ether and MP2100 can coat the mixing blades and cause batch-to-batch variation in water demand. The base coat is not intended for continuous immersion service, and water absorption is controlled separately by the hydrophobic additive and measured by EN 1015-18. Because the EAD qualification includes pull-off and transverse deformation tests on aged specimens, the MP2100 dosage is fixed only after a full ETA route is completed by the system holder, and published data for MP2100-specific ETA systems is limited outside manufacturer technical files.
Traffic-bearing repair mortars formulated to EN 1504-3:2005 classes R3 and R4 use ELOTEX MP2100 at 3.0–6.0 wt% in blends of Portland cement, silica fume or metakaolin, quartz sand, superplasticizer, and, where low-temperature placement is required, calcium nitrate or calcium formate accelerators. The mixing is performed in a pan mixer or a forced-action paddle mixer; the substrate is prepared by light bush hammering, grit blasting, or high-pressure water jetting to remove laitance and expose a sound concrete surface. The mortar is applied by trowel, low-pressure wet spraying, or hand packing when the void is small; wet thickness is usually kept below 25 mm per pass unless the formulation contains coarse sand to reduce exothermic heat. The working time is constrained because MP2100 increases water retention and extends wet film formation, while the accelerator and silica fume shorten initial set; field crews commonly observe that the open working window closes within 30–45 min at 30 °C unless the mix is shaded and mixed with chilled water. Tensile bond strength is verified by pull-off tests using EN 1542 on prepared concrete slabs; repair formulations containing 4.0 wt% MP2100 are typically designed to exceed the 2.0 MPa R4 requirement, but a formulation with 6.0 wt% polymer may reduce compressive strength below the 45 MPa R4 minimum if the water-to-binder ratio is not simultaneously reduced by superplasticizer adjustment. Published data for MP2100-specific R4 mortars is limited, so plant-level validation is conducted against EN 1504-3 type testing including capillary absorption, carbonation resistance, and thermal compatibility.
| Property | Test method | R3 requirement | R4 requirement |
| Compressive strength after 28 d | EN 12190 | ≥ 25 MPa | ≥ 45 MPa |
| Tensile bond strength to concrete | EN 1542 | ≥ 1.5 MPa | ≥ 2.0 MPa |
| Chloride ion content | EN 1015-17 | ≤ 0.05% | ≤ 0.05% |
| Carbonation resistance | EN 13295 | No requirement | dk ≤ reference concrete |
Plants use this matrix for raw material change control only; full R4 certification requires additional thermal compatibility and shrinkage testing under the harmonised EN 1504-3 route.
In one-component flexible cementitious waterproofing slurries applied beneath ceramic tile or as mineral waterproofing membranes, ELOTEX MP2100 is dry-blended at 5.0–8.0 wt% with Portland cement, limestone or quartz filler, fine sand, cellulose ether, and powdered superplasticizer. The powder mix is stirred into water using a slow-speed paddle mixer at 300–500 rpm for 2–3 min, allowed to slake for 5 min, and remixed. The resulting slurry is applied by brush, trowel, or notched squeegee in two coats with a total dry film thickness of 1.0–2.0 mm, with a polyester or glass fibre mesh embedded in the first coat where crack bridging is specified. Water impermeability is assessed under EN 14891:2017 for liquid-applied water impermeable products used under ceramic tiling; water absorption and crack bridging are evaluated after water immersion at 7 d and after heat ageing. The polymer loading at 6.0 wt% is usually the starting point for crack bridging applications because lower levels produce cement-rich films that fail in tension at the pretreated crack before the required deformation. A practical limitation is that MP2100-rich slurries do not re-disperse after cure; they form an irreversible coalesced polymer network when the water evaporates, so build-up in mixing vessels and pump hoppers must be mechanically removed. Acid chloride exposure should be avoided because vinyl acetate-ethylene copolymers soften or swell under ketone and ester solvents, which restricts the membrane to aqueous and alkaline service environments. Where the product is used as an exposed waterproofing layer, testing may shift to EN 1504-2 coating requirements; published data for MP2100 in that configuration is limited.
Gypsum-based joint fillers and repair compounds for plasterboard systems contain ELOTEX MP2100 at 1.0–3.0 wt% in formulations containing hemihydrate gypsum, finely ground calcium carbonate, talc, cellulose ether, and a retarder such as sodium citrate or a protein-based retarder. The dry mix is dispersed into water in a continuous mixer or by hand trowel mixing; the product is then applied over paper or fibre tape joints at a wet film thickness of 0.5–1.5 mm. The polymer powder contributes wet adhesion to the paper surface and controls incipient cracking in joints, but if the dosage exceeds 3.5 wt%, mechanical sanding becomes significantly more difficult because the film-forming polymer softens under the heat generated by orbital sanding discs and causes clogging of the abrasive. The cured compound is tested against EN 13279-1:2008 or EN 13963 jointing material requirements; setting time, flexural strength, and surface hardness are monitored, while sandability is assessed by a production-scale orbital sander with 180–240 grit paper rather than by bench tests alone. Chemical compatibility in gypsum systems requires careful selection of retarder: sodium citrate at 0.05–0.15 wt% delays crystallization sufficiently, but overdosing above 0.2 wt% interacts with the polyvinyl alcohol protective colloid of MP2100 and can extend final set beyond 120 min, making the compound unsuitable for same-day skim coating. Published data on MP2100-specific gypsum joint formulation is limited, and industrial validation typically uses EN 13279-1 type testing alongside full-scale sanding trials.
For large-format porcelain tile installations on low-absorbency screeds, cementitious tile grouts are formulated with ELOTEX MP2100 at 2.0–5.0 wt% when the target is a deformable grout conforming to EN 13888:2022 or ANSI A118.7. The dry blend contains white or grey Portland cement, calcium carbonate, fine silica sand, pigment, fluidizer, and, for water-repellent grouts, a stearate or silane additive. The powder is mixed with a defined water dose to a creamy consistency and applied with a rubber float; excess material is removed after initial stiffening, and the joint is finished with a damp sponge. The addition of MP2100 above 2.5 wt% reduces the water absorption of the cured grout and produces a slight deformation under lateral tile movement, which is useful when porcelain tiles are installed over heated screeds or low-absorption substrates with residual moisture. However, the polymer-rich grout also exhibits longer stain ingress during the first 72 h because the coalesced film blocks capillary pores but remains slightly hydrophilic; fast-track sealing is therefore delayed until full cure. The final hardened grout is checked for abrasion resistance according to EN 13888, with 3.0 wt% MP2100 as the typical plant baseline for a fine and smooth joint. The use of MP2100 in epoxy or furan grouts is outside the applicable scope, as redispersible powders are intended for cementitious binder systems only.
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ELOTEX MP2100 is a redispersible polymer powder based on a vinyl acetate-ethylene copolymer. The powder is manufactured by spray drying an aqueous dispersion stabilized with polyvinyl alcohol and protected by a mineral anticaking agent. It is a white to off-white free-flowing powder intended for dry-mix mortars. On addition of water, the dried dispersion particles redisperse; as the hydraulic binder sets and free water is consumed, the polymer particles coalesce into a continuous film. That film reinforces the mortar matrix and improves adhesion at interfaces with concrete, ceramic tile, and gypsum substrates. The product is used in cementitious tile adhesives, self-leveling flooring compounds, mineral repair mortars, and selected gypsum-based compounds requiring improved flexibility and adhesion without volatile coalescing agents.
The dry-mix handling behavior of ELOTEX MP2100 is controlled by bulk density, maximum particle size, residual moisture, and the content of noncombustible mineral residue. The bulk density range of 400–600 g/L requires gravimetric rather than volumetric feeding when mass-flow accuracy must remain within ±0.5 wt% of target polymer addition. The maximum particle size of ≤400 µm supports uniform distribution in dry blends, but the powder can segregate from fine mineral binders if subjected to excessive air transport or prolonged mixing. The minimum film formation temperature of 0 °C is determined by film-formation testing, while the glass transition temperature of 16 °C is determined by differential scanning calorimetry. The values listed below are representative technical data from the manufacturer’s specification sheet; shipment-specific values are controlled by the certificate of analysis.
| Parameter | Value | Reference method |
|---|---|---|
| Polymer basis | Vinyl acetate-ethylene copolymer | — |
| Stabilizer | Polyvinyl alcohol | — |
| Anticaking agent | Mineral filler | — |
| Appearance | White to off-white free-flowing powder | — |
| Bulk density | 400–600 g/L | ISO 60 |
| Maximum particle size | ≤400 µm | ISO 3310-1 |
| Residual moisture | ≤2 wt% | Manufacturer’s method |
| pH, 10% aqueous dispersion | 6.5–8.5 | ISO 976 |
| Minimum film formation temperature | 0 °C | ISO 2115 |
| Glass transition temperature | 16 °C | ISO 11357-2 |
| Residue on ignition | 10–14 wt% at 1000 °C | ISO 3451-1 |
Industrial dry-mix plants typically dose the powder through loss-in-weight feeders equipped with horizontal agitators. Volumetric auger dosing is not recommended as the sole control strategy because the bulk density range is broad enough to alter screw fill and discharge mass at constant speed. In a batch ploughshare mixer with a 1,000 kg dry charge, the powder is introduced after the first 60–90 s of mineral premixing. This sequence reduces the loss of low-density polymer particles into the dust-extraction stream and avoids the formation of polymer-rich agglomerates caused by direct contact with wet mixing water. If caking occurs during storage, the powder is screened through a 500 µm sieve; affected material should not be dried at elevated temperature because partial film formation may occur.
Mechanistically, redispersion begins when polyvinyl alcohol on the powder surface dissolves in mix water, releasing primary polymer particles. The mineral anticaking fraction is wetted and dispersed in the alkaline pore solution, where the pH rises rapidly to 12.5–13.5 as calcium hydroxide dissolves. The vinyl acetate-ethylene polymer remains stable under these alkaline conditions, but the acetate groups can undergo slow hydrolysis at temperatures above 40 °C; prolonged high-temperature mixing is therefore avoided. Film coalescence occurs after free water is consumed by hydration and evaporation. At a curing condition of 23 °C and 50% RH, the polymer phase can coalesce within 24–72 h, while cement hydration and strength development continue through 28 days. The resulting interpenetrating network of polymer and cement hydrates is responsible for the improved tensile adhesion and reduced brittleness observed in modified mortars.
In cementitious tile adhesives evaluated under EN 12004-1:2017+A1:2021 and classified through ISO 13007-2, ELOTEX MP2100 is used at typical addition rates of 1.5–4.0 wt% of dry mortar mass. The polymer increases low-shear viscosity and cohesion, allowing the adhesive to support wall tiles with limited slip. Slip resistance is measured according to EN 1308:2008; formulations containing MP2100 can be adjusted with cellulose ether rheology modifiers to remain below the 0.5 mm slip limit. Tensile adhesion strength is determined according to EN 1348:2008 after standard water immersion, heat ageing, and freeze-thaw cycling. MP2100 contributes to the polymer film required to maintain tensile adhesion values above the 0.5 N/mm² or 1.0 N/mm² thresholds associated with C1 and C2 classifications, respectively. The measured value is formulation-specific and depends on cement content, aggregate particle size distribution, air content, and substrate preparation.
Open-time extension is a second function. During the exposed tact time, the adhesive surface can lose tack by evaporative skinning. The redispersed vinyl acetate-ethylene particles coalesce into a thin polymer film at the surface, slowing water loss and preserving a deformable contact layer. Open-time testing under EN 1346:2008 typically reports tensile adhesion after a 30 min exposure interval; formulations with MP2100 are designed to retain values above 0.5 N/mm² at that interval when formulated for a C1 adhesive. The result is not an inherent property of the powder alone and must be verified on the complete adhesive formulation.
In self-leveling underlayments, the polymer is used at lower dosage than in tile adhesives because increasing polymer volume fraction can reduce flow and entrain air. The polymer improves flexural strength and crack-bridging, but the water demand is optimized with polycarboxylate ether superplasticizers. Industrial target flow spreads after mixing are commonly 140–160 mm using a ring spread test. This range is a formulation target rather than a direct property of the polymer powder.
A process conflict arises between polymer-induced air entrainment and hardened-mortar density. When MP2100 is added at high shear or with excessive mixing time, air content increases, which can reduce compressive strength and freeze-thaw durability. Defoamers are used to control entrained air, but overuse can destabilize the redispersed dispersion. On a plant scale, this is monitored by wet density measurement during mixing and by air content determination on fresh mortar according to EN 1015-7:1998.
The process window for tile adhesive production with MP2100 is constrained by the shear sensitivity of the powder. In high-intensity mixers operating with tip speeds above 20 m/s, localized heating and plastic deformation of the powder can produce agglomerates that persist after water addition. Low-speed batch mixers or ploughshare mixers are preferred; when high-shear dispersion is unavoidable, the polymer is added late and mixing time is minimized. Quality control uses a 1.0 mm sieve residue check on the dry blend; agglomerates larger than this size are rejected because they indicate poor dispersion or storage moisture ingress. Published data for the specific redispersion rate of MP2100 under continuous plastering-machine shear are limited.
Substituting a vinyl acetate homopolymer with MP2100 changes film-formation behavior at ambient temperature. Vinyl acetate homopolymers commonly exhibit a minimum film formation temperature above 15 °C; MP2100, with a minimum film formation temperature of 0 °C, forms a film at standard site temperatures without coalescing solvents. The ethylene comonomer provides internal plasticization, reducing stiffness and increasing deformability. In a repair mortar, this shift may improve adhesion to prepared concrete substrates after dry and wet storage, but the hardened surface can show lower scratch resistance and slightly higher recovery under load. Tensile properties are measured on formulated mortars rather than on the powder alone, so substitution studies are carried out at constant polymer volume fraction and constant water-to-binder ratio.
| Parameter | MP2100 vinyl acetate-ethylene | Vinyl acetate homopolymer | Styrene-butadiene powder |
|---|---|---|---|
| Glass transition temperature | 16 °C | 28–40 °C | −10–20 °C |
| Minimum film formation temperature | 0 °C | 15–20 °C | 0–5 °C |
| Water resistance | Moderate; improved by ethylene comonomer | Lower; acetate groups are more hydrophilic | Higher; hydrocarbon backbone is hydrolysis-resistant |
| Adhesion to damp concrete | High | Moderate | Moderate to high |
| Flexibility without external plasticizer | Medium | Low | Medium to high |
Compared with styrene-butadiene powders, vinyl acetate-ethylene polymers such as MP2100 generally provide stronger wet adhesion to concrete but lower resistance to prolonged water immersion and lower hydrolytic stability under warm alkaline ageing. Compared with higher-ethylene vinyl acetate-ethylene grades within the same brand family, MP2100 is positioned for applications requiring higher tensile strength and powder flow rather than maximum elongation. The selection of MP2100 over a vinyl acetate homopolymer is therefore justified when ambient film formation, wet adhesion, and flexibility are required without the use of external plasticizers or coalescents.
MP2100 is compatible with calcium formate, lithium carbonate, polycarboxylate ether superplasticizers, methyl cellulose ethers, starch ethers, and defoamers used in dry-mix formulations. The order of addition in laboratory mixing affects dispersion; the powder should be preblended with mineral components before adding water to prevent localized gelation. In high-alkali calcium sulfoaluminate-based systems, the rapid heat release can raise the paste temperature above 40 °C early in mixing; formulation trials are required because published data for this specific configuration are limited.
ELOTEX MP2100 should be stored in unopened paper bags or silos at temperatures below 35 °C and relative humidity below 70%. Exposure to relative humidity above 60% for prolonged intervals can produce lumps that do not redisperse; opened bags should be consumed promptly or sealed with moisture exclusion. The powder is incompatible with solvent-borne polymer systems and with strongly acidic accelerators that can destabilize the polyvinyl alcohol protective colloid. Compliance with regulatory requirements is assessed at the finished mortar level; relevant test standards include EN 998-1, EN 1504-3, ISO 13007-1, and EN 12004-1:2017+A1:2021. The powder itself is not a finished construction product and does not carry a CE marking under the Construction Products Regulation.
As an organic powder, MP2100 can form a combustible dust cloud in enclosed silos and conveying lines. Installations are subject to ATEX zone classification and should use grounded conductive components and dust extraction with antistatic filtration. This operational boundary applies to all organic redispersible powders.