Polyurea HYB
A two-component hybrid polyurea membrane, to be applied by spraying using a high-pressure bi-mixer pump for the on-site creation of a waterproofing membrane on various types of substrate.
A two-component hybrid polyurea membrane, to be applied by spraying using a high-pressure bi-mixer pump for the on-site creation of a waterproofing membrane on various types of substrate.
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Substrate preparation
Substrate preparation is essential; therefore, the surface to be treated must be free from any contaminants, dry, sound, and have a tensile strength of at least 1.5 MPa. In all cases, the floor surface must be prepared by milling, shot-blasting, grinding or sanding, depending on the type of surface.
Any free-standing or standing water originating from the substrate, previous washing operations or weather conditions must be removed or dried using appropriate methods. On porous substrates, the reactivity of the material and the resulting heat build-up could lead to the formation of through-holes in the coating due to the heating of air trapped within the surface.
It is therefore advisable to ensure, after applying the primer, that the surface is effectively sealed (saturated).
Primer
Preparation varies depending on the surface to be treated:
– Concrete surfaces: shot-blast, then skim-coat with Epox Grip loaded with 0.1–0.3 mm quartz. For very porous surfaces, apply a double skim-coat.
– Fresh resin: dust with quartz sand to improve the product’s adhesion. On damp surfaces or where there is counter-pressure, apply Rasoepoxy until a dry surface is achieved, then apply a further coat and dust with quartz.
– On heavily corrugated areas, the surface can be levelled by applying Rasoepoxy with 0.1–0.3 or 0.1–0.5 quartz added to adjust both the thickness and consistency of the product.
– Metal surfaces: dry-blast in accordance with SSPC-SP10 to Sa2.5 grade and coat immediately with Polyurea HYB.
– To create surfaces with a certain degree of slip resistance, immediately after applying the first coat of Polyurea HYB, rotate the spray gun so that it is parallel to the surface to be treated, keep the nozzle pointing upwards and move the arm in a sweeping motion to create a ‘shower’ of Polyurea HYB.
Product preparation and application
Mix component A thoroughly before spraying. Two-component product, applicable using a high-pressure bi-mixer airless system, preferably PLC-controlled for dosing and flow rate, fitted with a suitable mixing gun for polyurethane systems (in-gun reaction). Best performance is achieved by spraying the product at a temperature of 75–80°C for component A and 70–75°C for component B, at pressures of 170 to 190 bar (data measured at the spray gun).
The equipment must be fitted with in-line heaters, heated tanks and hoses. The components of POLYUREA HYB must not be contaminated with any chemical agents (solvents, oils, water or anything else) as this would seriously compromise the product’s characteristics.
For applications under tiles, apply 200–250 g/m² of Polyurea Primer Rapid to Polyurea HYB, dusted with quartz of a suitable grain size. Once cured, we recommend using a single-component adhesive for external use, class C2TE S1, or a flexible two-component product.
When kept in its original sealed packaging, stored in a dry, protected place at a temperature between +6°C and +30°C, the product has a shelf life of 12 months.
Do not store the product at temperatures below +6°C.
If the product is to be applied to roofs with insulation or other compressible surfaces, particularly during the winter months, it is necessary to wait approximately 6–8 hours for the product to cure completely before it is safe to walk on.
| Color | Code | Bicomponent | Packaging size | Barcode |
|---|---|---|---|---|
| Bright grey | 8461 * | 2 components | 435 kg | |
| Bright grey | 8464 * | 2 components | 116 kg |
| Density of Component A | 1.05 ± 0.05 kg/l | EN ISO 2811-1 |
| Density of Component B | 1.05 ± 0.05 kg/l | EN ISO 2811-1 |
| Viscosity at 25 °C Component A | 600 ± 100 mPas | EN ISO 2555 |
| Viscosity at 25 °C Component B | 1200 ± 250 mPas | EN ISO 2555 |
| Parameter | Value | Reference standard |
|---|---|---|
| Mixing ratio (by weight) | 100:107 | – |
| Theoretical consumption | 2.2 kg/m² | – |
| Theoretical thickness | 2 mm | – |
| Non-volatile solids | > 99.8 % | EN ISO 3251 |
| Adhesion to concrete | > 3.0 MPa | EN 1542 |
| Adhesion to metal | > 7.0 MPa | EN 13144 |
| Adhesion to fibre cement | > 1.4 MPa | EN 1542 |
| Thermal shock resistance | > 3.3 MPa | EN 13687-5 |
| Tensile strength | > 19 MPa | EN 12311-2 |
| Tear resistance | > 12 kN/m | EN 12310-2 |
| Maximum elongation | > 480 % | EN 12311-2 |
| Tensile strength, -20°C | > 14.3 MPa | EN 12311-2 |
| Maximum deformation, -20°C | > 114 % | EN 12311-2 |
| Shore D hardness | > 42 | EN ISO 868 |
| Mass drop | 20 N·m | EN ISO 6272 |
| Abrasion resistance (Taber) | < 35 mg (Mola H22, 1000 g, 1000 revolutions) | EN ISO 5470-1 |
| Crack bridging Method A, static Method B, dynamic | A5 (23°C) no cracking > B4.1 (23°C) no cracking | EN 1062-7 |
| Water absorption | w < 0.1 kg/m² × h⁰·⁵ | EN 1062-3 |
| Ozone resistance | Excellent | EN 1844 |
| Chemical resistance: | ||
| Hydrocarbon mixture | Class II | EN 13529 |
| 10% acetic acid | Class II | |
| Sulphuric acid 20 % | Class II | |
| Sodium hydroxide 20 % | Class II | |
| Sodium chloride 20 % | Class II |
SUMMARY OF CONSUMPTION PER CYCLE:
Dry or slightly damp concrete surface
1 or 2 coats of Epox Grip filled with 30% quartz (0.1–0.3 mm)
Sprinkle with 0.5–0.8 mm quartz (while still wet)
1 coat ofPolyurea HYB
→ 300–500 g/m² consumption per coat of binder
→ approx. 2000 g/m² (quartz)
→ approx. 1100 g/m² (Polyurea HYB)
Surface in wet concrete or on a counter-slab, low temperatures
2 coats of Rasoepoxy filled with 30% 0.1–0.3 mm quartz, diluted with 10% water
Sprinkle with 0.5–0.8 mm quartz (while still wet)
1 coat ofPolyurea HYB
→ 400–600 g/m² consumption per coat of binder
→ approx. 2000 g/m² (quartz)
→ approx. 1100 g/m² (Polyurea HYB)
Note: Consumption figures are indicative; actual consumption depends on numerous factors, including the surface’s absorbency and roughness profile.
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