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The Electrical Double Layer & DLVO Theory

Colloids stay dispersed because a charged double layer surrounds each particle and repels its neighbours. Understanding that double layer, and the DLVO balance of forces, is the foundation of all coagulation design.

The Electrical Double Layer & Zeta Potential

Colloidal particles in water carry a negative surface charge that surrounds them with a cloud of counter-ions — the electrical double layer — which keeps them mutually repelled and stably suspended. The strength of that repulsion is measured as zeta potential, and stable colloids typically sit between −15 and −40 mV. Coagulation works by compressing or neutralising this double layer so attractive van der Waals forces can dominate and particles can aggregate. Understanding the double layer explains why coagulant dose, pH and ionic strength behave as they do, and underpins the jar-testing and dose-control decisions we make on every clarification design.

Why Colloids Stay Apart

Surface Charge

Clay, organics, oil droplets and cells carry a net negative surface charge, giving a zeta potential typically between minus 15 and minus 30 mV.

The Double Layer

A bound Stern layer and a diffuse layer of counter-ions surround each particle, creating an electrostatic repulsion that prevents contact.

DLVO Balance

DLVO theory sums attractive van der Waals and repulsive electrostatic energies; the net barrier height decides whether particles aggregate.

Collapsing the Repulsion Barrier

Compressing the Layer

Raising ionic strength compresses the diffuse layer and lowers the energy barrier to aggregation.

Neutralising Charge

Coagulants drive zeta potential toward zero (minus 5 to plus 5 mV), removing the repulsion so particles stick on first collision.

Reaching the Minimum

Once the barrier falls, particles fall into the primary energy minimum and aggregate irreversibly.

From Theory to Dose

Zeta Measurement

Streaming-current and zeta-potential measurement guide coagulant dose to the charge-neutral point.

Charge Demand

Particle and organic concentration set the charge demand and therefore the coagulant requirement.

Process Selection

The required mechanism, neutralisation or sweep, follows directly from the colloidal chemistry.

Optimising a coagulation and flocculation process?

Reynolds & Bauhm delivers this scope as part of an integrated, single-point engagement matched to your project, programme and regulatory regime.

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