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Capillary Flow Porometry (CFP)

Capillary flow porometry (CFP) is an analytical technique that uses controlled displacement of liquid via inert gases to characterize the through-pores in wettable materials such as membranes, filtration media, and other permeable or semipermeable materials.

What Is Capillary Flow Porometry (CFP)?

Capillary flow porometry is optimal for analyzing pores that directly contribute to fluid transport (open, permeable, or through-pores). It has a wide dynamic range of measurable pore sizes and the unique ability to determine through-pore gas permeability and bubble point. Measurements of larger pores are much faster than acquiring gas adsorption isotherms (~30 minutes versus 8-24 hours), which is necessary for nanoscale porous materials.

Other details:

  • Must be a solid material with gas-permeable through-pores.
  • Must be completely wettable by a liquid suitable for analysis.
  • Pore size range between ~ 0.02 to 500 µm.
  • Must be sealable using an O-ring – not too rough and rigid.

Rapid Measurements

Rapid Measurements

Ideal for applications like filtration media.

Non-Destructive

Non-Destructive

Non-destructive and non-toxic analysis conditions.

Wide Measurement Range

Wide Measurement Range

Wide dynamic measurement range.

Why Use CFP?

  • Pore size and gas permeability determination of through-pores in permeable materials.
  • Determine the pore size distribution in the size range of: ~0.02 to 500 µm.
  • Bubble point, cumulative flow percent, and pore density determination.

Measure the Pores That Matter

Analyze only open, flow-relevant through-pores.

Fast, Non-Destructive Testing

Get accurate results in minutes, not hours.

Full Performance Insight

Assess pore size, bubble point, and gas permeability.

Covalent’s Capabilities Offer CFP for Through‑Pore Size Analysis

Covalent Capabilities

Working Principle

A porometry measurement involves first thoroughly wetting the sample with an appropriate wetting solution. This fluid fills the pores and blocks gas from flowing through them via capillary forces that are described by the Washburn equation:
​​
D=(4γ∙cosθ)/ΔP

where D is the pore/capillary diameter, is the known surface tension of the wetting liquid, θ is the contact angle between the liquid and pore surface / capillary wall (should be 0° if fully wetted), and ΔP is the differential gas pressure applied by the porometer.

The sample is sealed between a mesh support screen and an O-ring. Gas pressure is then directionally applied and ramped up. As the gas pressure increases, the wetting fluid is evacuated from more and more pores, with larger pores emptying first due to the lower capillary forces holding the wetting fluid inside. A dry run without the wetting fluid is also performed to determine which phase in the wet run aligns with when the pores have fully evacuated.

Equipment Used for CFP:

At Covalent, we use Anton Paar / Quantachrome’s highest-end  3G zH capillary flow porometer.

Anton Paar Porometer 3G zh

Key specifications:

  • Minimum Detectable Pore Size: 13 nm.
  • Maximum Detectable Pore Size: 500 μm.
  • Flow Rate Range: 0.01 to 200 L/min.
  • Flow Sensor Temperature Coefficient: < 0.5% / °C
    (from 15 to 45 °C).
  • Maximum Pressure: up to 500 psi (34.5 bar).
  • Pressure Accuracy: ± 0.05% f.s.
View Spec Sheet
Anton Paar Porometer 3G zh capillary flow porometer – high‑end instrument used for capillary flow porometry measurements of pore size and gas flow characteristics

Key Differentiators

Strengths

  • Rapid and reproducible measurements are ideal for applications like filtration media.
  • Generally non-destructive and non-toxic analysis conditions.
  • Wide dynamic range of measurable pore sizes.
  • Only measures open, permeable pores which are relevant to fluid transport.

Limitations

  • Not suitable for nanoporous materials (< 20 nm).
  • Pore density must not be excessively restrictive to flow.
  • Pores must be open and through-connected, i.e., permeable with gas flow.
Covalent Expert Consultation

Unsure Whether CFP Is Right for You?

Learn more about using CFP services today.

Sample Information

Example capillary flow porometry (CFP) pore size distribution graph showing cumulative pore number per cm² versus pore size (µm) for membrane samples F1 and F2, illustrating pore size range and total porosity

Example Pore Size Distribution for two samples, ‘F1’ (red), and ‘F2’ (gray). The calculated cumulative number of pores per unit cm2 is plotted as a function of Pore Size in microns. Sample F1 shows a higher proportion of pores with size < 10 μm, and Sample F2 shows a broader distribution of pore sizes (from 10 to 55 μm) as well as a greater total porosity.

Example capillary flow porometry (CFP) cumulative pore flow and differential pore flow percentage graph versus pore diameter (µm) for samples F1 and F2, highlighting minimum, maximum, and average through‑pore diameters.

Example plot of cumulative flow % and differential flow % contrast with pore size for the same two samples shown above. These plots are computed from the raw flow rate data and can be used to analyze minimum, maximum, and average pore sizes in each sample. Sample F1 has average through-pore diameter of 9.5 μm and Sample F2 has an average through-pore diameter of approximately 33 μm.

Raw flow rate versus pressure capillary flow porometry (CFP) graph showing wet and dry flow curves for filter samples F1 and F2, comparing wet-flow liquid displacement and dry-flow gas measurements in bar and L/min

Raw Flow Rate versus Pressure data for the samples F1 and F2 shown above. These are collected in two phases: a wet-flow state (during liquid displacement) and dry flow state (after all liquid is removed).

What we accept?

The sample must be a solid material with gas-permeable through-pores. The standard size is 25 mm with a maximum thickness of 3 mm (other configurations may be possible). The sample must be completely wettable by a liquid suitable for analysis. A pore size range between ~0.02 – 500 µm is generally accepted. The sample must be sealable using an O-ring; not too rough and rigid, but able to withstand 100+ psi of gas pressure during analysis.

Use Cases

Complementary Techniques

  • Gas adsorption or BET: Gas adsorption is another Porosimetry technique optimal for analyzing solid materials’ specific surface area and pore size distribution with pores of all types, ranging from approximately 0.35 to 50 nm in size.
  • Mercury Intrusion Porosimetry (MIP): This technique is very similar and complementary to porometry, although it analyzes all types of pores, including nanoscale pores. It can obtain surface area, total porosity, and pore size distributions.
  • Solid Surface Zeta Potential: The surface charge of fabrics, textiles, and, in some cases, membranes can play a key role in their performance, alongside the characterization of the through-pores in these materials via capillary flow porometry.

Zeta Potential

Electric potential at the slipping plane of the EDL. Explore

Gas Adsorption Porosimetry

Characterizes porous materials. Explore

Why Choose Covalent for Your CFP Needs?

We offer several complementary techniques for completely characterizing the pores in our clients’ materials of interest and other physical and chemical properties related to the material performance. At Covalent, we can prepare samples in-house to make them measurable and ultimately deliver the valuable data you need.

Frequently Asked Questions

Identifying the right test can be complex, but it doesn’t have to be complicated.
Here are some questions we are frequently asked.