Skip to main content
Calcimator

Emulsion Stability Calculator

Calculate HLB blend ratios, creaming velocity (Stokes' Law), and emulsion type for food emulsion formulation.

About this calculator

Two independent physics problems live in this calculator, and both matter for whether an emulsion holds together on the shelf. The first is emulsifier selection via HLB (hydrophilic-lipophilic balance): given the HLB your oil phase requires and the HLB of two emulsifiers you have on hand, it solves the linear blend equation required HLB = x×HLB_A + (1−x)×HLB_B for the weight fraction x, telling you exactly how much of each surfactant to combine. HLB below about 7 favors water-in-oil emulsions, above 8 favors oil-in-water, and the calculator flags which regime your target falls into.

The second problem is physical stability, addressed through Stokes' Law: creaming or sedimentation velocity scales with the square of droplet radius, so halving droplet size (through better homogenization) cuts separation velocity to a quarter, not a half — a nonlinear payoff that's easy to underestimate. That velocity, combined with the density difference between phases and continuous-phase viscosity, is converted into an estimated time for a visible 1 cm layer to separate, which is what most people actually care about rather than a raw velocity number in μm/s. Because Stokes' Law assumes dilute, non-interacting spherical droplets, it will overstate stability for concentrated or flocculating emulsions — treat the separation-time estimate as an optimistic baseline to validate against a real accelerated-stability trial, not a substitute for one.

Inputs

%

Results

Emulsifier A (%)

48.54

Emulsifier B (%)51.46
Achieved blend HLB10
Creaming velocity (μm/s)1.09
Time to separate 1 cm (hrs)2.5
Emulsion type3
Phase volume ratio (O:W)0.43
How to Use This Calculator
  1. Enter the required HLB for your oil phase and the HLB values for your two emulsifiers.
  2. Set droplet diameter, density difference, and continuous phase viscosity.
  3. Enter oil phase percentage.
  4. The calculator shows emulsifier A/B blend percentages, achieved HLB, creaming velocity, estimated separation time, emulsion type, and phase volume ratio.
  5. Use emulsifier percentages to formulate the blend and creaming velocity to predict stability before a physical stability trial.

How the result changes with Required HLB

Required HLBEmulsifier A (%)
597.09
7.572.82
150
200

What each input means

Required HLB
Target HLB value for the oil phase. Look up required HLB for your specific oil (e.g., mineral oil 12, soybean oil 7).
Emulsifier A HLB
HLB of low-HLB emulsifier (e.g., Span 80 = 4.3, GMS = 3.8).
Emulsifier B HLB
HLB of high-HLB emulsifier (e.g., Tween 80 = 15.0, Tween 20 = 16.7).
Droplet diameter (μm)
Average emulsion droplet diameter in micrometers. Smaller = more stable.
Density difference (kg/m³)
Absolute density difference between oil and water phases (~80 kg/m³ for vegetable oils).
Continuous phase viscosity (Pa·s)
Viscosity of the continuous phase. Water ≈ 0.001 Pa·s, thickened sauce ≈ 0.1 Pa·s.
Oil phase (%)
Volume percentage of the oil (dispersed) phase.

What each result means

Emulsifier A (%)
Weight percentage of emulsifier A in the blend to achieve the target HLB.
Emulsifier B (%)
Weight percentage of emulsifier B in the blend.
Achieved blend HLB
Actual HLB of the emulsifier blend.
Creaming velocity (μm/s)
Stokes' Law separation velocity. Lower = more stable emulsion.
Time to separate 1 cm (hrs)
Estimated hours for visible separation of a 1 cm layer. -1 = effectively stable.
Emulsion type
1 = W/O (water-in-oil), 2 = borderline, 3 = O/W (oil-in-water).
Phase volume ratio (O:W)
Oil to water phase volume ratio.

How this is calculated

Worked example, using the default values

  1. Identify Input Parameters
    4 parameters
    Required HLB = 10, Emulsifier A HLB = 4.7, Emulsifier B HLB = 15, Droplet diameter (μm) = 5 = 7 input(s) provided
  2. Calculate Emulsifier A
    48.54 = 48.54
  3. Calculate Emulsifier B
    Emulsifier B = 1 - fractionA
    51.46 = 51.46
  4. Calculate Achieved blend HLB
    Achieved blend HLB = fractionA * emulsifierAHlb + fractionB * emulsifierBHlb
    10 = 10

Engine last updated . Checked against 3 independently-derived tests — how we verify calculators. Built by Paul Gunder, a software engineer, not a licensed financial, medical, or legal professional.

Frequently Asked Questions

How does the calculator figure out what ratio of my two emulsifiers to use?

It solves the HLB blend equation algebraically: since the target HLB is a weighted average of the two emulsifier HLBs, x = (requiredHLB - HLB_B) / (HLB_A - HLB_B) gives the weight fraction of emulsifier A directly. The remaining fraction (1 - x) becomes emulsifier B, and the calculator clamps the result between 0 and 1 so it never recommends a negative or over-100% blend.

Why does halving the droplet size cut the creaming velocity to a quarter instead of half?

The Stokes' Law formula in this calculator includes droplet radius squared, so creaming velocity scales with the square of droplet size, not linearly. Halving the radius through better homogenization reduces that squared term to one-quarter of its original value, which is why smaller droplets deliver disproportionately better shelf stability than the size reduction alone would suggest.

My emulsion type shows 2 = borderline. What does that mean for formulation?

The calculator classifies your required HLB into three regimes: below 7 favors water-in-oil emulsions, above 8 favors oil-in-water, and 7-8 sits in a borderline zone where either emulsion type can form depending on other factors like phase ratio and processing. A borderline required HLB usually means small formulation changes, like a different emulsifier blend or oil phase ratio, can flip which emulsion type you actually get, so it's worth testing rather than assuming.

Why might my actual emulsion separate faster than the calculated time to separate 1 cm predicts?

The creaming-velocity math assumes dilute, non-interacting spherical droplets, which is the classic Stokes' Law assumption, but real emulsions above roughly 20-30% dispersed phase or with flocculating droplets interact hydrodynamically and separate faster than isolated spheres would. Treat the calculated separation time as an optimistic best case and confirm actual shelf stability with an accelerated physical trial, especially at higher oil-phase percentages.

The questions that sit next to this one — chosen by subject, including calculators filed under a different category.

More in Cooking, Food & Beverage.