Assess
Assess water analysis and saturation risk
Scale & deposits
Control mineral deposits in cooling water, membranes and process installations.
From problem to cause
Deposit risk is determined by concentration, pH, temperature, residence time, local evaporation and mixing. The best solution combines chemistry with process settings.
Approach
Assess water analysis and saturation risk
Determine critical temperature and concentration zones
Select chemistry and operating limits
Verify performance using trends and inspection
Root-cause diagnosis
We therefore link visible signs to water chemistry, process data, materials and the location where the problem occurs in the installation.
Hardness, alkalinity, pH, temperature and cycles of concentration jointly determine the risk of carbonate scale.
Not every hard deposit is carbonate scale. Its composition determines the appropriate prevention and cleaning method.
Particles can settle, consume inhibitor and provide a base for further fouling.
Treatment route
Frequently asked questions
These answers provide initial direction. The final approach follows from the installation data and product documentation.
No. Silica, calcium phosphate, gypsum, metal oxides and combinations with organic matter can also be light in colour. Analysis prevents the wrong cleaning choice.
An antiscalant is primarily preventive. Existing deposits often require separate, controlled cleaning and correction of the cause.
Local wall temperature, the concentration boundary layer and evaporation may be less favourable there than in a bulk sample of the circulating water.
A specific challenge?
Briefly describe what you observe in the installation. Together, we will determine the most logical first step.